(S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

Base Information

Chemical Name:(S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester
CAS No.:161867-54-5
Molecular Formula:C₂₄H₃₉NO₈Si
Molecular Weight:497.661
Hs Code.:

(S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

Synonyms:(S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

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Chemical Property of (S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

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Technology Process of (S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

There total 2 articles about (S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester 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: 90.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 160147-88-6
methyl 2-benzyloxycarbonylamino-2-deoxy-3,4-O-isopropylidene-D-mannonate

: 161867-54-5
(S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 0 ℃;
DOI:10.1016/0040-4039(94)88373-4

Reference yield:

: 160147-87-5
methyl 2-benzyloxycarbonylamino-2-deoxy-3,4:5,6-di-O-isopropylidene-D-mannonate

: 161867-54-5
(S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / Dowex 50W-X₈ (110 W/Wpercent) / methanol; H₂O / 27 h / Ambient temperature

2: 90 percent / imidazol / dimethylformamide / 0 °C

With 1H-imidazole; Dowex 50W-X₈ (110 W/Wpercent); In methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(94)88373-4

Reference yield:

: 161867-54-5
(S)-Benzyloxycarbonylamino-{(4R,5R)-5-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-acetic acid methyl ester

: 161867-56-7
Methanesulfonic acid (R)-1-[(4S,5R)-5-((R)-1-benzyloxycarbonylamino-2-hydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(tert-butyl-dimethyl-silanyloxy)-ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / tetrahydrofuran / Ambient temperature

2: 91 percent / LiAlH₄ / tetrahydrofuran / 0 °C

With lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1016/0040-4039(94)88373-4