Some tips on 19752-55-7

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 1-Bromo-3,5-dichlorobenzene, other downstream synthetic routes, hurry up and to see.

Reference of 19752-55-7, The chemical industry reduces the impact on the environment during synthesis 19752-55-7, name is 1-Bromo-3,5-dichlorobenzene, I believe this compound will play a more active role in future production and life.

N*3*-(3,5-Dichloro-phenyl)-l,N*5*-bis-(4-methoxy-benzyl)-N*5*-methyl-lH- [l,2,4]triazole-3,5-diamine In a 25 mL sealed tube, sodium tert-butoxide (97.9 mg, 1.02 mmol, Eq: 1.20), bis(dibenzylideneacetone)palladium (48.8 mg, 84.9 muiotaetaomicron, Eq: 0.1) and 2-di-tert-butylphosphino- 2′,4′,6′-triisopropylbiphenyl (36.0 mg, 84.9 muiotaetaomicron, Eq: 0.1) were combined with toluene (5 mL) to give a dark brown suspension. N5,l-bis(4-methoxybenzyl)-N5-methyl-lH-l,2,4-triazole-3,5- diamine (300 mg, 849 muiotaetaomicron, Eq: 1.00) and l-bromo-3,5-dichlorobenzene (230 mg, 1.02 mmol, Eq: 1.20) were added. The reaction mixture was degassed with argon for 15 min, and then heated to 110°C for 3 hours. The reaction mixture was cooled and diluted with EtOAc (50 mL), washed with H20 (25 mL) and brine (25 mL). The organic layer was dried over anhydrous MgS04, filtered and volatiles were removed under reduced pressure to yield an oil from which the compound was isolated by column chromatography (Hexanes/EtOAc = 70/30) to give an off- white solid 140 mg (33percent). MH+ 498.2

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 1-Bromo-3,5-dichlorobenzene, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; F. HOFFMANN-LA ROCHE AG; HOFFMANN-LA ROCHE INC.; DING, Qingjie; JIANG, Nan; WEIKERT, Robert James; WO2014/135472; (2014); A1;,
Chloride – Wikipedia,
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