(2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate

Base Information

• Chemical Name: (2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate
• CAS No.: 910448-06-5
• Molecular Formula: C₃₅H₅₄N₂O₇SSi
• Molecular Weight: 674.974

Synonyms:(2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate

Chemical Property of (2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate

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Technology Process of (2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate

There total 2 articles about (2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate 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: 64.0%

(2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylthio)pyrrolidine-1-carboxylate (910448-05-4) → (2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate (910448-06-5)

Guidance literature:

With Oxone; In methanol; water; at 20 ℃; for 0.5h;

Reference yield: 64.0%

(S)-N-((1R,2S)-1-((2R,4R)-4-(4-fluorobenzyloxy)pyrrolidin-2-yl)-3-(3,5-difluorophenyl)-1-hydroxypropan-2-yl)-2-((S)-3-acetamido-3-((S)-sec-butyl)-2-oxopyrrolidin-1-yl)-4-phenylbutanamide → C35H54N2O6SSi + (2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate (910448-06-5)

Guidance literature:

With oxone; In methanol; water; at 20 ℃; for 0.5h;

Reference yield: 99.0%

(2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate (910448-06-5) → (2R,4R)-tert-butyl 2-((1S,2S)-2-amino-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate (877079-59-9)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In methanol; for 3h; under 2585.81 Torr; Parr apparatus;

upstream raw materials:

(2R,4R)-tert-butyl 2-((1S,2S)-2-(benzyloxycarbonylamino)-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylthio)pyrrolidine-1-carboxylate

Downstream raw materials:

(2R,4R)-tert-butyl 2-((1S,2S)-2-amino-1-(tert-butyldimethylsilyloxy)-3-phenylpropyl)-4-(propylsulfonyl)pyrrolidine-1-carboxylate

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