(S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide

Base Information

Chemical Name:(S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide
CAS No.:161708-84-5
Molecular Formula:C₃₀H₂₉N₃O₄S
Molecular Weight:527.644
Hs Code.:

Synonyms:(S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide

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Chemical Property of (S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide

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Technology Process of (S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide

There total 4 articles about (S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide 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:

: 61535-47-5,58889-48-8
benzyl (S)-(1-hydroxy-3-(1H-indol-3-yl)propan-2-yl)carbamate

: 161708-84-5
(S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1: H₂ / 5percent Pd/C / tetrahydrofuran; methanol / 3 h / 760 Torr / Ambient temperature

2: HOBt, WSC / dimethylformamide / 14 h / Ambient temperature

3: H₂ / 5percent Pd/C / tetrahydrofuran; methanol / 3 h / 760 Torr / Ambient temperature

4: 4-N,N-dimethylaminopyridine / dimethylformamide / 2 h

With dmap; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm9803065

Reference yield:

: 161708-61-8
N-benzyloxycarbonyl-(L)-phenylalanyl-(L)-tryptophanol

: 161708-84-5
(S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 5percent Pd/C / tetrahydrofuran; methanol / 3 h / 760 Torr / Ambient temperature

2: 4-N,N-dimethylaminopyridine / dimethylformamide / 2 h

With dmap; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm9803065

Reference yield:

: 154-09-6,526-53-4,2899-29-8,52485-52-6
L-tryptophanol

: 161708-84-5
(S)-N-[(S)-1-Hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-2-(naphthalene-1-sulfonylamino)-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: HOBt, WSC / dimethylformamide / 14 h / Ambient temperature

2: H₂ / 5percent Pd/C / tetrahydrofuran; methanol / 3 h / 760 Torr / Ambient temperature

3: 4-N,N-dimethylaminopyridine / dimethylformamide / 2 h

With dmap; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm9803065