(3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

Base Information

Chemical Name:(3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide
CAS No.:1049832-66-7
Molecular Formula:C₂₀H₁₈ClN₃O₂
Molecular Weight:367.835
Hs Code.:

Synonyms:(3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

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Technology Process of (3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

There total 6 articles about (3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide 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: 80.0%

: 79-04-9
chloroacetyl chloride

: 1049832-33-8
(3S)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

: 1049832-66-7
(3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

Guidance literature:: With triethylamine; In 1,4-dioxane; at 20 ℃; for 1h;

Reference yield:

: 243842-54-8
(3S)-1-phenyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid methyl ester

: 1049832-66-7
(3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: ammonia / methanol / 26 h / 20 °C

2: triethylamine / 1,4-dioxane / 1 h / 20 °C

With ammonia; triethylamine; In 1,4-dioxane; methanol;

Reference yield:

: 4299-70-1
L-tryptophan methyl ester

: 1049832-66-7
(3S)-2-(chloroacetyl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluoroacetic acid / benzene / 1 h / Heating / reflux; Molecular sieve

2.1: trifluoroacetic acid / benzene / 3 h / Heating / reflux; Molecular sieve

2.2: 20 °C / pH 8

3.1: ammonia / methanol / 26 h / 20 °C

4.1: triethylamine / 1,4-dioxane / 1 h / 20 °C

With ammonia; triethylamine; trifluoroacetic acid; In 1,4-dioxane; methanol; benzene; 1.1: Pictet-Spengler Cyclisation / 2.1: Pictet-Spengler Cyclisation;