1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine

Base Information

Chemical Name:1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine
CAS No.:127648-97-9
Molecular Formula:C₂₄H₂₂BrFN₄O₂S
Molecular Weight:529.433
Hs Code.:

Synonyms:1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine

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Chemical Property of 1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine

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Technology Process of 1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine

There total 4 articles about 1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 83737-97-7
1-methyl-2-(aminomethyl)-5-(2'-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine

: 2-bromoacetamidothiophene-3-carbonyl chloride

: 127648-97-9
1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine

Guidance literature:: With triethylamine; In dichloromethane; at -20 ℃; for 18h;
DOI:10.1016/0223-5234(89)90022-6

Reference yield:

: 4651-81-4
Methyl 2-aminothiophene-3-carboxylate

: 127648-97-9
1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / triethylamine / CH₂Cl₂ / 20 h / -20 °C

2: 400 mg / BBr₃ / CH₂Cl₂ / 20 h / Heating

3: SOCl₂ / 0.5 h / Heating

4: 88 percent / triethylamine / CH₂Cl₂ / 18 h / -20 °C

With thionyl chloride; boron tribromide; triethylamine; In dichloromethane;
DOI:10.1016/0223-5234(89)90022-6

Reference yield:

: 127648-94-6
methyl-2-bromoacetamidothiophene-3-carboxylate

: 127648-97-9
1-methyl-2-(2'-bromoacetamidothiophene-3-carboxamido)-methyl-5-(2'-fluorophenyl)-2H-1,4-benzodiazepine

Guidance literature:: Multi-step reaction with 3 steps

1: 400 mg / BBr₃ / CH₂Cl₂ / 20 h / Heating

2: SOCl₂ / 0.5 h / Heating

3: 88 percent / triethylamine / CH₂Cl₂ / 18 h / -20 °C

With thionyl chloride; boron tribromide; triethylamine; In dichloromethane;
DOI:10.1016/0223-5234(89)90022-6