1H-1,4-Benzodiazepine-1-acetic acid, 5-(2-fluorophenyl)-2,3-dihydro-3-(1H-indol-3-ylmethyl)-2-oxo-, ethyl ester, (R)-

Base Information

Chemical Name:1H-1,4-Benzodiazepine-1-acetic acid, 5-(2-fluorophenyl)-2,3-dihydro-3-(1H-indol-3-ylmethyl)-2-oxo-, ethyl ester, (R)-
CAS No.:103343-11-9
Molecular Formula:C28H24FN3O3
Molecular Weight:469.515
Hs Code.:
Mol file:103343-11-9.mol

Synonyms:

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Chemical Property of 1H-1,4-Benzodiazepine-1-acetic acid, 5-(2-fluorophenyl)-2,3-dihydro-3-(1H-indol-3-ylmethyl)-2-oxo-, ethyl ester, (R)-

Chemical Property:

Purity/Quality:

Safty Information:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-1,4-Benzodiazepine-1-acetic acid, 5-(2-fluorophenyl)-2,3-dihydro-3-(1H-indol-3-ylmethyl)-2-oxo-, ethyl ester, (R)-

There total 5 articles about 1H-1,4-Benzodiazepine-1-acetic acid, 5-(2-fluorophenyl)-2,3-dihydro-3-(1H-indol-3-ylmethyl)-2-oxo-, ethyl ester, (R)- 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:

: 1581-13-1
2-amino-2'-fluorobenzophenone

: 103343-11-9
1,3-Dihydro-1-(ethoxycarbonylmethyl)-5-(2-fluorophenyl)-3(R)-(3'-indolyl)methyl-2H-1,4-benzodiazepin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 2 h / 0 °C

2: aq. NaOH / methanol / 72 h

3: 1.) NaH / 1.) DMF, 0 deg C, 40 min, 2.) DMF, from 0 deg C to RT, 20 min

With sodium hydroxide; sodium hydride; In tetrahydrofuran; methanol;
DOI:10.1021/jm00390a019

Reference yield:

: 103222-66-8
D-tryptophan acid chloride hydrochloride

: 103343-11-9
1,3-Dihydro-1-(ethoxycarbonylmethyl)-5-(2-fluorophenyl)-3(R)-(3'-indolyl)methyl-2H-1,4-benzodiazepin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 2 h / 0 °C

2: aq. NaOH / methanol / 72 h

3: 1.) NaH / 1.) DMF, 0 deg C, 40 min, 2.) DMF, from 0 deg C to RT, 20 min

With sodium hydroxide; sodium hydride; In tetrahydrofuran; methanol;
DOI:10.1021/jm00390a019

Reference yield:

: 103342-80-9
2-N-(D-tryptophanyl)amino-2'-fluorobenzophenonehydrochloride

: 103343-11-9
1,3-Dihydro-1-(ethoxycarbonylmethyl)-5-(2-fluorophenyl)-3(R)-(3'-indolyl)methyl-2H-1,4-benzodiazepin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / methanol / 72 h

2: 1.) NaH / 1.) DMF, 0 deg C, 40 min, 2.) DMF, from 0 deg C to RT, 20 min

With sodium hydroxide; sodium hydride; In methanol;
DOI:10.1021/jm00390a019