(1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ⁴-[1,4]thiazepane-3-carboxylic acid benzhydryl ester

Base Information

• Chemical Name: (1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ⁴-[1,4]thiazepane-3-carboxylic acid benzhydryl ester
• CAS No.: 77628-17-2
• Molecular Formula: C₄₅H₅₁N₃O₉S
• Molecular Weight: 809.981

Synonyms:(1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ⁴-[1,4]thiazepane-3-carboxylic acid benzhydryl ester

Chemical Property of (1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ⁴-[1,4]thiazepane-3-carboxylic acid benzhydryl ester

Chemical Property:

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Technology Process of (1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ⁴-[1,4]thiazepane-3-carboxylic acid benzhydryl ester

There total 3 articles about (1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ⁴-[1,4]thiazepane-3-carboxylic acid benzhydryl 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: 98.0%

(3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-5-oxo-[1,4]thiazepane-3-carboxylic acid benzhydryl ester (77628-15-0) → (1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ4-[1,4]thiazepane-3-carboxylic acid benzhydryl ester (77628-17-2)

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 0.5h;

DOI:10.1139/v81-062

Reference yield:

Nα-(tert-butyloxycarbonyl)-L-α-aminoadipic acid α-benzhydryl ester (71264-14-7) → (1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ4-[1,4]thiazepane-3-carboxylic acid benzhydryl ester (77628-17-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 84 percent / N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline

2: 98 percent / 85percent m-chloroperoxybenzoic acid / CH₂Cl₂ / 0.5 h / 0 °C

With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;

DOI:10.1139/v81-062

Reference yield:

3D-benzhydryloxycarbonyl-6L-amino-2,2-dimethyl-5-oxoperhydro-1,4-thiazepine (77628-10-5) → (1R,3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-1,5-dioxo-1λ4-[1,4]thiazepane-3-carboxylic acid benzhydryl ester (77628-17-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline / 1.) ethyl acetate, 5 min; 2.) 72 h

2: 98 percent / 85percent m-chloroperoxybenzoic acid / CH₂Cl₂ / 0.5 h / 0 °C

With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;

DOI:10.1139/v81-062

upstream raw materials:

(3S,6R)-6-((S)-5-Benzhydryloxycarbonyl-5-tert-butoxycarbonylamino-pentanoylamino)-2,2-dimethyl-5-oxo-[1,4]thiazepane-3-carboxylic acid benzhydryl ester

N^α-(tert-butyloxycarbonyl)-L-α-aminoadipic acid α-benzhydryl ester

3D-benzhydryloxycarbonyl-6L-amino-2,2-dimethyl-5-oxoperhydro-1,4-thiazepine

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