[4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride

Base Information

Chemical Name:[4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride
CAS No.:1228935-09-8
Molecular Formula:C₂₆H₁₉ClN₆O₂
Molecular Weight:482.929
Hs Code.:

Synonyms:[4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride

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Chemical Property of [4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride

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Technology Process of [4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride

There total 4 articles about [4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride 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:

: 1228935-06-5
[4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetic acid

: 1228935-09-8
[4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride

Guidance literature:: With thionyl chloride; N,N-dimethyl-formamide; at 20 ℃; for 1h;

Reference yield:

: 1228935-05-4
tert-butyl 3-{[6-(2-tert-butoxy-2-oxoethyl)-5-oxo-1-phenyl-5,6-dihydro-4H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-4-yl]methyl}-1H-indazole-1-carboxylate

: 1228935-09-8
[4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 20 °C

2: thionyl chloride / N,N-dimethyl-formamide / 1 h / 20 °C

With thionyl chloride; trifluoroacetic acid; N,N-dimethyl-formamide; In dichloromethane;

Reference yield:

: (5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl)-acetic acid tert-butyl ester

: 1228935-09-8
[4-(1H-indazol-3-yl-methyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]acetyl chloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium t-butanolate / N,N-dimethyl-formamide / 0 - 20 °C / Sonication

1.2: -50 - 20 °C

2.1: trifluoroacetic acid / dichloromethane / 20 °C

3.1: thionyl chloride / N,N-dimethyl-formamide / 1 h / 20 °C

With thionyl chloride; trifluoroacetic acid; sodium t-butanolate; N,N-dimethyl-formamide; In dichloromethane; N,N-dimethyl-formamide;