4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH

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Chemical Name:4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH
CAS No.:190834-01-6
Molecular Formula:C₃₈H₄₈ClN₃O₈S₂
Molecular Weight:774.399
Hs Code.:

Synonyms:4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH

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Chemical Property of 4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH

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Technology Process of 4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH

There total 8 articles about 4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH 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: 34.0%

: 190834-00-5
4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OCH3

: 190834-01-6
4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH

Guidance literature:: With sodium hydroxide; In ethanol; at 60 ℃; for 20h;
DOI:10.1021/jm960772z

Reference yield:

: 950-59-4
4-hydroxy-3,5-di-tert-butylthiophenol

: 190834-01-6
4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / K₂CO₃

2: 30 percent / NaOH / ethanol

3: 66 percent / Et₃N, HOBT, DCC / dimethylformamide / 20 h

4: 34 percent / aq. NaOH / ethanol / 20 h / 60 °C

With sodium hydroxide; potassium carbonate; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm960772z

Reference yield:

: 27894-50-4
methyl (2S)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoate hydrochloride

: 190834-01-6
4-({[(4-chlorophenyl)sulfonyl]amino}carbonyl)benzoyl-N-ε-{[(4-hydroxy-3,5-di-tert-butylphenyl)thio]butyroyl}-Lys-OH

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / BOP, DIEA / dimethylformamide / 18 h / Ambient temperature

2: HBr, AcOH / 4 h

3: 66 percent / Et₃N, HOBT, DCC / dimethylformamide / 20 h

4: 34 percent / aq. NaOH / ethanol / 20 h / 60 °C

With sodium hydroxide; hydrogen bromide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm960772z