(4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

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Chemical Name:(4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
CAS No.:365449-63-4
Molecular Formula:C₄₃H₅₄N₂O₁₀
Molecular Weight:758.909
Hs Code.:

(4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Synonyms:(4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

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Chemical Property of (4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

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Technology Process of (4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

There total 6 articles about (4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl 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: 87.0%

: 100-39-0
benzyl bromide

: 540770-29-4
(4S,5S)-5-{(S)-Benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-4-carboxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 365449-63-4
(4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: (4S,5S)-5-{(S)-Benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-4-carboxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester; With caesium carbonate; In methanol; water; for 0.5h;

benzyl bromide; In N,N-dimethyl-formamide; at 0 ℃; for 6h; Further stages.;
DOI:10.1021/ol0101279

Reference yield:

: 540770-27-2
(4S,5S)-4-Allyl-5-((S)-1-benzyloxy-2-oxo-ethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 365449-63-4
(4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 98 percent / NaClO₂; NaH₂PO₄*H₂O; 2-methyl-2-butene / 2-methyl-propan-2-ol; H₂O

2.1: EDCI; DMAP / CH₂Cl₂ / 12 h / 23 °C

3.1: O₃ / CH₂Cl₂ / -78 - 23 °C

4.1: NaClO₂; NaH₂PO₄*H₂O; 2-methyl-2-butene / 2-methyl-propan-2-ol; H₂O

5.1: Cs₂CO₃ / methanol; H₂O / 0.5 h

5.2: 87 percent / dimethylformamide / 6 h / 0 °C

With dmap; sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; caesium carbonate; ozone; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/ol0101279

Reference yield:

: 365449-52-1
(4S,5S)-4-Allyl-5-((S)-benzyloxy-carboxy-methyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 365449-63-4
(4S,5S)-4-Benzyloxycarbonylmethyl-5-{(S)-benzyloxy-[(S)-1-((S)-8-methoxy-1-oxo-isochroman-3-yl)-3-methyl-butylcarbamoyl]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: EDCI; DMAP / CH₂Cl₂ / 12 h / 23 °C

2.1: O₃ / CH₂Cl₂ / -78 - 23 °C

3.1: NaClO₂; NaH₂PO₄*H₂O; 2-methyl-2-butene / 2-methyl-propan-2-ol; H₂O

4.1: Cs₂CO₃ / methanol; H₂O / 0.5 h

4.2: 87 percent / dimethylformamide / 6 h / 0 °C

With dmap; sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; caesium carbonate; ozone; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/ol0101279