(S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate

Base Information

Chemical Name:(S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate
CAS No.:1445828-50-1
Molecular Formula:C₃₈H₄₅N₅O₅
Molecular Weight:651.806
Hs Code.:

Synonyms:(S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate

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Chemical Property of (S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate

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Technology Process of (S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate

There total 7 articles about (S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)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: 40.0%

: 1445778-88-0
(S)-1-(4-amino-2-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)-N,N-dibutyl-5-methyl-1H-pyrazole-3-carboxamide

: 501-53-1,94274-21-2
benzyl chloroformate

: 1445828-50-1
(S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate

Guidance literature:: With potassium carbonate; In dichloromethane; at 20 ℃; for 5h;

Reference yield:

: 1445778-86-8
(S)-1-(2-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)-4-nitrophenyl)-5-methyl-1H-pyrazole-3-carboxylic acid

: 1445828-50-1
(S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 12 h / 20 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 5 h / 20 °C

3: potassium carbonate / dichloromethane / 5 h / 20 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1445778-87-9
(S)-N,N-dibutyl-1-(2-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)-4-nitrophenyl)-5-methyl-1H-pyrazole-3-carboxamide

: 1445828-50-1
(S)-benzyl (4-(3-(dibutylcarbamoyl)-5-methyl-1H-pyrazol-1-yl)-3-(3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / ethanol / 5 h / 20 °C

2: potassium carbonate / dichloromethane / 5 h / 20 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; In ethanol; dichloromethane;