(3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester
CAS No.:210752-16-2
Molecular Formula:C₃₅H₃₉F₃N₂O₇
Molecular Weight:656.699
Hs Code.:

Synonyms:(3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

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Chemical Property of (3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

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Technology Process of (3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

There total 12 articles about (3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-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: 44.0%

: 20445-33-4,39637-99-5
(R)-methoxytrifluoromethylphenylacetyl chloride

: (3R,4R)-3-(4-Benzyloxy-benzoylamino)-4-hydroxy-azepane-1-carboxylic acid tert-butyl ester

: 210752-14-0
(3R,4R)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

: 210752-16-2
(3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; for 7.5h; Ambient temperature;
DOI:10.1021/jo980208r

Reference yield:

: 210752-10-6
(4-Hydroxy-butylamino)-acetaldehyde O-benzyl-oxime

: 210752-16-2
(3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: Na₂CO₃ / acetone; H₂O / 5 h / Heating

2: CrO₃, pyridine / CH₂Cl₂ / 0.25 h / Ambient temperature

3: Bu₃SnH, AIBN / benzene / 8 h / Heating

4: hydrogen / PtO₂ / methanol / 5 h

5: 58 percent / NaHCO₃ / CH₂Cl₂; H₂O / 2.5 h / Ambient temperature

6: 44 percent / Et₃N, DMAP / CH₂Cl₂ / 7.5 h / Ambient temperature

With pyridine; chromium(VI) oxide; dmap; 2,2'-azobis(isobutyronitrile); hydrogen; tri-n-butyl-tin hydride; sodium hydrogencarbonate; sodium carbonate; triethylamine; platinum(IV) oxide; In methanol; dichloromethane; water; acetone; benzene;
DOI:10.1021/jo980208r

Reference yield:

: 210752-12-8
(2-Benzyloxyimino-ethyl)-(4-hydroxy-butyl)-carbamic acid tert-butyl ester

: 210752-16-2
(3S,4S)-3-(4-Benzyloxy-benzoylamino)-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: CrO₃, pyridine / CH₂Cl₂ / 0.25 h / Ambient temperature

2: Bu₃SnH, AIBN / benzene / 8 h / Heating

3: hydrogen / PtO₂ / methanol / 5 h

4: 58 percent / NaHCO₃ / CH₂Cl₂; H₂O / 2.5 h / Ambient temperature

5: 44 percent / Et₃N, DMAP / CH₂Cl₂ / 7.5 h / Ambient temperature

With pyridine; chromium(VI) oxide; dmap; 2,2'-azobis(isobutyronitrile); hydrogen; tri-n-butyl-tin hydride; sodium hydrogencarbonate; triethylamine; platinum(IV) oxide; In methanol; dichloromethane; water; benzene;
DOI:10.1021/jo980208r