(S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol

Base Information

Chemical Name:(S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol
CAS No.:1239876-78-8
Molecular Formula:C₂₃H₂₄N₂O₆S
Molecular Weight:456.519
Hs Code.:

Synonyms:(S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol

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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 (S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol

Chemical Property:

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Technology Process of (S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol

There total 4 articles about (S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol 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:

: 1239876-77-7
C₂HF₃O₂*C₁₅H₁₈N₂O₄S

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

: 1239876-78-8
(S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol

Guidance literature:: With sodium hydrogencarbonate; In water; ethyl acetate; at 0 - 20 ℃;

Reference yield:

: C₁₅H₁₈N₂O₄S

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

: 1239876-78-8
(S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol

Guidance literature:: With sodium hydrogencarbonate; In water; ethyl acetate; at 0 - 20 ℃; for 1.5h;
DOI:10.1002/hc.21256

Reference yield:

: 1623-92-3
4-phenoxyphenylsulfonyl chloride

: 1239876-78-8
(S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfonamido)propanol

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 2 h / 0 - 20 °C

2: trifluoroacetic acid / methanol; chloroform / 2.5 h / 0 °C

3: sodium hydrogencarbonate / water; ethyl acetate / 1.5 h / 0 - 20 °C

With sodium hydrogencarbonate; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; chloroform; water; ethyl acetate;
DOI:10.1002/hc.21256