phenylmethyl <1S-<1R(R),2S,3R>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>carbamate

Base Information

Chemical Name:phenylmethyl <1S-<1R*(R*),2S*,3R*>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>carbamate
CAS No.:135760-03-1
Molecular Formula:C₃₃H₅₀N₄O₇S
Molecular Weight:646.849
Hs Code.:

phenylmethyl <1S-<1R*(R*),2S*,3R*>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>carbamate

Synonyms:phenylmethyl <1S-<1R*(R*),2S*,3R*>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>carbamate

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Chemical Property of phenylmethyl <1S-<1R*(R*),2S*,3R*>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>carbamate

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Technology Process of phenylmethyl <1S-<1R*(R*),2S*,3R*>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>carbamate

There total 8 articles about phenylmethyl <1S-<1R*(R*),2S*,3R*>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>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: 73.0%

: 122621-77-6
(2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane

: 135704-24-4
N-<(1,1-dimethylethoxy)carbonyl>-3-<2-<<(phenylmethoxy)carbonyl>amino>-4-thiazolyl>-L-alanine

: 135760-03-1
phenylmethyl <1S-<1R*(R*),2S*,3R*>>-<4-<3-<<1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl>amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>-3-oxopropyl>-2-thiazolyl>carbamate

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm00092a006

Reference yield:

: 122621-77-6
(2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane

: 135704-23-3,135704-24-4
(R)-3-(2-Benzyloxycarbonylamino-thiazol-4-yl)-2-tert-butoxycarbonylamino-propionic acid

: 135703-71-8,135760-03-1
{4-[(R)-2-tert-Butoxycarbonylamino-2-((1S,2R,3S)-1-cyclohexylmethyl-2,3-dihydroxy-5-methyl-hexylcarbamoyl)-ethyl]-thiazol-2-yl}-carbamic acid benzyl ester

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm00092a006

Reference yield:

: 132286-86-3
(R)-3-(2-Amino-thiazol-4-yl)-2-tert-butoxycarbonylamino-propionic acid benzyl ester

: 135703-71-8,135760-03-1
{4-[(R)-2-tert-Butoxycarbonylamino-2-((1S,2R,3S)-1-cyclohexylmethyl-2,3-dihydroxy-5-methyl-hexylcarbamoyl)-ethyl]-thiazol-2-yl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: aq. sodium bicarbonate / tetrahydrofuran; CH₂Cl₂ / Ambient temperature

2: aq. KOH / ethanol / 4 h / Ambient temperature

3: N-hydroxybenzotriazole (HOBT), dicyclohexylcarbodiimide (DCC) / dimethylformamide / 0 - 20 °C

With potassium hydroxide; sodium hydrogencarbonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00092a006