(S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

Base Information

Chemical Name:(S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate
CAS No.:1584150-21-9
Molecular Formula:C₂₃H₂₆ClN₃O₃
Molecular Weight:427.931
Hs Code.:

Synonyms:(S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

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Chemical Property of (S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

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Technology Process of (S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

There total 5 articles about (S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate 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: 48.0%

: 1798-85-2
1-bromo-3-cyclopropylbenzene

: 1584150-10-6
(S)-tert-butyl (9-chloro-2-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

: 1584150-21-9
(S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium carbonate; XPhos; In tert-butyl alcohol; at 80 ℃; Inert atmosphere;

Reference yield:

: 64182-61-2
1-chloro-3-fluoro-2-nitrobenzene

: 1584150-21-9
(S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / ethanol / 9 h / 80 °C / Inert atmosphere

2: ammonium chloride; ethanol; iron / water / 1.5 h / 80 °C

3: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine / N,N-dimethyl-formamide / 3 h

4: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; potassium carbonate / tert-butyl alcohol / 80 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; ethanol; iron; potassium carbonate; ammonium chloride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; XPhos; In ethanol; water; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 76387-70-7
(S)-3-amino-2-tert-butoxycarbonylaminopropionic acid

: 1584150-21-9
(S)-tert-butyl (6-chloro-1-(3-cyclopropylphenyl)-4-oxo-2,3,4,5-tetrahydro-1H-benzo-[b][1,4]-diazepin-3-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / ethanol / 9 h / 80 °C / Inert atmosphere

2: ammonium chloride; ethanol; iron / water / 1.5 h / 80 °C

3: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine / N,N-dimethyl-formamide / 3 h

4: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; potassium carbonate / tert-butyl alcohol / 80 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; ethanol; iron; potassium carbonate; ammonium chloride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; XPhos; In ethanol; water; N,N-dimethyl-formamide; tert-butyl alcohol;