Category: chlorides-buliding-blocks

Application of 106131-61-7, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 106131-61-7, name is 3,6-Dichloro-1,2,4,5-tetrazine belongs to chlorides-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

Compound 5 (1.5 g, 1 mol) And tetraethylene glycol monomethyl ether (3.16ml, 1.5mol) were dissolved in 50ml of dichloromethane, Triethylamine (2.96 ml, 1.5 mol) was then added. After stirring at room temperature for 3 hours, The reaction was quenched with water, extracted with dichloromethane, dried and passed through a silica gel column. Compound 6b (2.8 g, 87%) was obtained.

The synthetic route of 3,6-Dichloro-1,2,4,5-tetrazine has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Chinese Academy Of Sciences Chemical Institute; Yang Guoqiang; Zhao Zhensheng; Wang Shuangqing; Hu Rui; Li Shayu; (12 pag.)CN107286186; (2017); A;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Reference of 627-42-9, These common heterocyclic compound, 627-42-9, name is 2-Methoxyethyl chloride, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

A solution of ethyl 3,4-dihydroxybenzoate (1.7 g, 9.3 mmol) was placed in a reaction flask and 8 mL of DMF was added to dissolve it. Potassium tert-butoxide (2.0 g, 17.8 mmol) and potassium iodide (1.0 g, 6.0 mmol), and the temperature was raised to 100 C. 2-Chloroethyl methyl ether (3.52 g, 37.2 mmol) was added dropwise and the reaction was continued for 12 h after completion of the dropwise addition. Cooled to room temperature, ice water (200 mL) was added, and extracted three times with ethyl acetate (3 x 200 mL). The organic phase was combined, washed three times with distilled water, three times with saturated brine, dried over anhydrous sodium sulfate overnight, filtered, and the filtrate was evaporated to dryness under reduced pressure to give an oil. The elution system was petroleum ether / ethyl acetate = 1) Ethyl 3,4-bis (2-methoxyethoxy) benzoate.

Statistics shows that 2-Methoxyethyl chloride is playing an increasingly important role. we look forward to future research findings about 627-42-9.

Reference:
Patent; Shandong University; Shandong Yikang Pharmaceutical Co., Ltd.; Zhao Guisen; Li Pengzhan; Shi Yongqiang; Yin Yanzhen; Wang Yongtao; (11 pag.)CN104725327; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Related Products of 104-11-0, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 104-11-0 as follows.

To a solution under nitrogen gas of 2,4-dichloroquinoline (1.00 g, 5.0 mmol) in dry THF (10 ml) was added 4-chloro-N-methylbenzylamine (1.57 g, 10.1 mmol, 2 eq.) and t-BuONa (1.36 g, 14.1 mmol, 2.8 eq.). The resulting mixture was degassed 5 min with nitrogen, then Xantphos (292 mg, 0.51 mmol, 0.1 eq.) and Pd(OAc)2 (57 mg, 0.25 mmol) were added and the reaction mixture was heated under reflux for 3 h. The reaction mixture was then cooled to room temperature and concentrated under reduced pressure. The residue was partitioned between brine and AcOEt and the aqueous layer was extracted with AcOEt. The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure to give a brown oil. The crude product was purified by flash chromatography (gradient Petroleum ether/DCM from 5/5 to 0/10) to give 800 mg (yield 50%) of a brown solid corresponding to 2-(4-chloro-N-methylbenzylamino)-4- chloroquinoline. Mass: (ES+) C17H14Cl2N2, required 317; found 317-319 [M+H], HPLC/MS method 1.

According to the analysis of related databases, 104-11-0, the application of this compound in the production field has become more and more popular.

Reference:
Patent; GENOSCIENCE PHARMA; BRUN, Sonia; BERET, Antoine; BASSISSI, Firas; HALFON, Philippe; COURCAMBECK, Jerome; (275 pag.)WO2017/191599; (2017); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Reference of 202197-26-0, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 202197-26-0 as follows.

Compound 12 (1.6 g, 6.28 mmol), commercially available 3-chloro-4-(3-fluorobenzyloxy)aniline 13 (1.6 g, 6.3 mmol) and CH3SO3H (20 muL, 5 mol %) were added into anhydrous EtOH (40 mL) and the reaction mixture was heated at 70 C for 2 h. After cooled down, the alcohol solution was diluted with water (150 mL) and the resulting solid was filtered, washed with water and dried to give N-(3-chloro-4-((3-fluorobenzyl)oxy)phenyl)-5-iodo-6-methylpyrimidin-4-amine 14 (2.77 g, 94%) as a white solid. MS-ESI (m/z): 467.8(M-H), 470.0(M+H); 1H NMR (CDCl3, delta): 2.65(s, 3H), 5.15(s, 2H), 6.94(d, 1H), 7.02(t, 1H), 7.16(d, 1H), 7.22(d, 1H), 7.35(d, 2H), 7.67(s, 1H), 8.39(s, 1H).

According to the analysis of related databases, 202197-26-0, the application of this compound in the production field has become more and more popular.

Reference:
Article; Mao, Yongjun; Zhu, Wenxiu; Kong, Xiaoguang; Wang, Zhen; Xie, Hua; Ding, Jian; Terrett, Nicholas Kenneth; Shen, Jingkang; Bioorganic and Medicinal Chemistry; vol. 21; 11; (2013); p. 3090 – 3104;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

53145-38-3, name is 2-Chloro-6-fluoroanisole, belongs to chlorides-buliding-blocks compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. COA of Formula: C7H6ClFO

4. Preparation of 4-chloro-2-fluoro-3-methoxybenzoic acid To a magnetically stirred solution of 2-chloro-6-fluoroanisole (16.06 g) in 100 mL of anhydrous DME, cooled to -70 C., was added 44 mL of 2.5 M n-BuLi in hexanes over 30 min, while keeping the reaction temperature below -55 C. After stirring the reaction for an additional 60 min at -70 C., dry carbon dioxide was bubbled into the reaction mixture for 60 min, while keeping the temperature below -60 C. Upon warming to room temperature, the reaction mixture was added to 150 mL of ether and acidified with 37% aq. HCl. The aqueous layer was washed with 2*150 mL of ether, and the combined organic layers were washed with sat. NaCl and were dried (Mg2SO4). Solvent removal gave 20.3 g of a white solid, which was recrystallized from ether/hexane to give 16.4 g (80% yield) of 4-chloro-2-fluoro-3-methoxybenzoic acid; MP 183-184 C.; 1H NMR (d6-DMSO, 300 MHz) delta 13.5 (brs, 1H), 7.60 (dd, 1H, J=1.8, 8.8 Hz), 7.42 (dd, 1H, J=1.8, 8.8 Hz), 3.95 (s, 3H).

The synthetic route of 53145-38-3 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Dow AgroSciences LLC; US2009/182168; (2009); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Reference of 1871-57-4,Some common heterocyclic compound, 1871-57-4, name is 3-Chloro-2-chloromethyl-1-propene, molecular formula is C4H6Cl2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

To a stirred suspension of sodium hydride (60% suspension in oil) (1.74 g, 43.5 mmol) in N,N-dimethylformamide (36 mL) at 0 C. was added 2-chloro-2-(chloromethyl)prop-1-ene (1.54 mL, 14.5 mmol). To this was added tert-butyl N-[2-(tert-butoxycarbonylamino)ethyl]carbamate (3.78 g, 14.5 mmol) in THF (36 mL). After 15 minutes the ice-bath was removed and the reaction stirred at room temperature for 18 h. The reaction was quenched by the addition of saturated ammonium chloride (100 mL) and the mixture concentrated to remove the THF. The aqueous was extracted with EtOAc (3×) and the combined organics were dried (MgSO4) and the solvent evaporated to afford a crude solid. This was purified (silica, 0 to 20% EtOAc/i-hexane) to afford the title compound as a white solid (2.24 g, 49%). 1H NMR (300 MHz, CDCl3) 1.45 (18H, s), 3.45 (4H, m), 3.90 (2H, m), 4.0 (2H, m), 4.95 (2H, m).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 3-Chloro-2-chloromethyl-1-propene, its application will become more common.

Reference:
Patent; BicycleTx Limited; Beswick, Paul; Mudd, Gemma Elizabeth; McDonnell, Kevin; Ivanova-Berndt, Gabriela; Van Rietschoten, Katerine; Witty, David; Skynner, Michael; US2020/131228; (2020); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Electric Literature of 918538-05-3,Some common heterocyclic compound, 918538-05-3, name is 2,4-Dichloropyrrolo[2,1-f][1,2,4]triazine, molecular formula is C6H3Cl2N3, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Compound 5 (80 mg, 0.424 mmol) was weighed out,P-trifluoromethoxybenzeneboronic acid (90 mg, 0.44 mmol)Triethylamine (121 mg, 1.2 mmol)Bis (triphenylphosphine) palladium (II) chloride (30 mg, 0.042 mmol)DMF (28.5 ml), water (0.5 ml) was added to the flask and heated to 80 C for 4 h.After stopping the reaction, 100 ml of water was added to the reaction solution,Stirred, extracted with ethyl acetate (20 ml * 4)The ester layer was dried over anhydrous sodium sulfate, concentrated,Column chromatography (petroleum ether: ethyl acetate = 20: 1) gave a yellow solid (97 mg, 77.6%).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 2,4-Dichloropyrrolo[2,1-f][1,2,4]triazine, its application will become more common.

Reference:
Patent; Jiangsu Xiansheng Pharmaceutical Co., Ltd.; Xin Minxing; Wen Jun; Tu Chongxing; Liu Zhaoyu; Shen Han; Wang Mengyu; Zhao Xinge; (36 pag.)CN104003990; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 139512-70-2, name is 4-Chloro-5-fluorobenzene-1,2-diamine belongs to chlorides-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below. category: chlorides-buliding-blocks

[4-(5-Chloro-6-fluoro-1H-benzoimidazol-2-yl)-phenyl]-methyl-(2-piperidin-1-yl-ethyl)-amine mp 167-168 C.

The synthetic route of 139512-70-2 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Millennium Pharmaceuticals, Inc.; US6348487; (2002); B1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Electric Literature of 38762-41-3, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 38762-41-3 as follows.

f) Compound 1.7; A solution of 4-bromo-2-chloroaniline (4.00 g, 19.37 mmol), bis(pinacolato)diboron (5.90 g, 23.2 mmol) and KOAc (12.3 g, 58.1 mmol) in DMSO (100 mL) was deoxygenated by bubbling nitrogen through it for 45 min. PdCl2 (dppf) g, 1.94 mmol) and dppf (1.07 g, 1.94 mmol) were then added and the mixture was heated at 100C for 4 h. After cooling to room temperature the reaction mixture was diluted with EtOAc, washed successively with water and brine, dried (MgS04), filtered and concentrated under reduced pressure. The crude product was purified twice by flash chromatography using CH2Cl2 to give intermediate 1.7 (2.15 g, 44% yield) as a white solid.

According to the analysis of related databases, 38762-41-3, the application of this compound in the production field has become more and more popular.

Reference:
Patent; BOEHRINGER INGELHEIM INTERNATIONAL GmbH; BOEHRINGER INGELHEIM PHARMA GmbH & CO KG; WO2005/118575; (2005); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Related Products of 7149-75-9, A common heterocyclic compound, 7149-75-9, name is 4-Chloro-3-methylaniline, molecular formula is C7H8ClN, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Step 1 (0420) To a mixture of 4-chloro-3-methylphenylamine (350 mg), potassium carbonate (1.09 g) and N,N-dimethylformamide (10 mL) was added trifluoromethanesulfonic acid 2,2,2-trifluoroethyl ester (0.57 mL), and the mixture was stirred at an external temperature of 80° C. for 20 hours. The mixture was cooled to room temperature. After the mixture was diluted with ethyl acetate, and the resulting mixture was washed with water, saturated sodium hydrogen carbonate aqueous solution and brine successively, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: 0percent-10percent ethyl acetate:hexane, gradient elution) to give (4-chloro-3-methylphenyl)-(2,2,2-trifluoroethyl)amine (209 mg). (0421) 1H-NMR (CDCl3) delta ppm: 2.31 (3H, s), 3.65-3.90 (3H, m), 6.46 (1H, dd, J=8.5, 2.8 Hz), 6.55 (1H, d, J=2.8 Hz), 7.15 (1H, d, J=8.5 Hz).

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; Kissei Pharmaceutical Co., Ltd.; Inoue, Hitoshi; Ohno, Kohsuke; Nakamura, Tetsuya; Ohsawa, Yusuke; (58 pag.)US2016/362368; (2016); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics