<5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid

Base Information

Chemical Name:<5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid
CAS No.:159589-37-4
Molecular Formula:C₃₁H₂₇N₃O₄
Molecular Weight:505.573
Hs Code.:

Synonyms:<5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid

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Chemical Property of <5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid

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Technology Process of <5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid

There total 8 articles about <5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid 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: 94.0%

: 159589-35-2
ethyl <5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetate

: 159589-37-4
<5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; for 18h; Ambient temperature;
DOI:10.1248/cpb.46.1566

Reference yield:

: 6516-89-8
2,3,4,5-tetrahydro-1H-1,5-benzodiazepine

: 159589-37-4
<5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 87 percent / Et₃N / CH₂Cl₂ / 0.5 h / 0 - 5 °C

2: 51 percent / K₂CO₃ / dimethylformamide / 18 h / 100 °C

3: 98 percent / H₂ / 10 percent Pd/C / acetic acid / 760 Torr / Ambient temperature

4: Et₃N / CH₂Cl₂ / 0.5 h / Ambient temperature

5: 94 percent / 1 N NaOH / tetrahydrofuran / 18 h / Ambient temperature

With sodium hydroxide; hydrogen; potassium carbonate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.1248/cpb.46.1566

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 159589-37-4
<5-<4-(2-phenylbenzoylamino)benzoyl>-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl>acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 87 percent / Et₃N / CH₂Cl₂ / 0.5 h / 0 - 5 °C

2: 51 percent / K₂CO₃ / dimethylformamide / 18 h / 100 °C

3: 98 percent / H₂ / 10 percent Pd/C / acetic acid / 760 Torr / Ambient temperature

4: Et₃N / CH₂Cl₂ / 0.5 h / Ambient temperature

5: 94 percent / 1 N NaOH / tetrahydrofuran / 18 h / Ambient temperature

With sodium hydroxide; hydrogen; potassium carbonate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.1248/cpb.46.1566