phenylmethyl [(2R,3S)-3-({[3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)phenyl]carbonyl}amino)-2-hydroxy-4-phenylbutyl]methylcarbamate

Base Information

Chemical Name:phenylmethyl [(2R,3S)-3-({[3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)phenyl]carbonyl}amino)-2-hydroxy-4-phenylbutyl]methylcarbamate
CAS No.:1031361-57-5
Molecular Formula:C₃₂H₄₀N₄O₆S
Molecular Weight:608.759
Hs Code.:

phenylmethyl [(2R,3S)-3-({[3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)phenyl]carbonyl}amino)-2-hydroxy-4-phenylbutyl]methylcarbamate

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Chemical Property of phenylmethyl [(2R,3S)-3-({[3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)phenyl]carbonyl}amino)-2-hydroxy-4-phenylbutyl]methylcarbamate

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Technology Process of phenylmethyl [(2R,3S)-3-({[3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)phenyl]carbonyl}amino)-2-hydroxy-4-phenylbutyl]methylcarbamate

There total 1 articles about phenylmethyl [(2R,3S)-3-({[3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)phenyl]carbonyl}amino)-2-hydroxy-4-phenylbutyl]methylcarbamate 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:

: 1079994-12-9
phenylmethyl [(2R,3S)-3-amino-2-hydroxy-4-phenylbutyl]methylcarbamate hydrochloride

: 811785-77-0
3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)benzoic acid

: 1031361-57-5
phenylmethyl [(2R,3S)-3-({[3-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-5-(ethylamino)phenyl]carbonyl}amino)-2-hydroxy-4-phenylbutyl]methylcarbamate

Guidance literature:: With N-ethylmorpholine;; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; at 20 ℃; for 16h;
DOI:10.1021/jm800138h