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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216291Generated: October 25, 2026

Benzene → tert-butyl 2-[({(2R,3S)-2-hydroxy-3-[((2S)-3-methyl-2-{3-[(2-methyl-1,3-thiazol-4-yl)methyl]-2-oxoimidazolidin-1-yl}butanoyl)amino]-4-phenylbutyl}amino)methyl]pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/216291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactanttert-butyl (2S)-2-formylpyrrolidine-1-carboxylateHCID 2734674—
ReactantSodium borohydrideHCID 4311764—
Reactant(2S)-N-[(1S,2R)-3-amino-1-benzyl-2-hydroxypropyl]-3-methyl-2-{3-[(2-methyl-1,3-thiazol-4-yl)methyl]-2-oxoimidazolidin-1-yl}butanamideHCID 66891621—
SolventEthanolHCID 702—
Producttert-butyl 2-[({(2R,3S)-2-hydroxy-3-[((2S)-3-methyl-2-{3-[(2-methyl-1,3-thiazol-4-yl)methyl]-2-oxoimidazolidin-1-yl}butanoyl)amino]-4-phenylbutyl}amino)methyl]pyrrolidine-1-carboxylateHCID 66891972103%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of the product of Example 274C (59 mg) in ethanol:benzene (1 mL, 1:1) was treated with N-t-butoxylcarbonyl-(L)-prolinal (26 mg, 1 equivalent), stirred at 70° C. for 1 hour, cooled at 25° C., treated with NaBH4 (14 mg, 3 equivalents) at 25° C. and stirred for 16 hours. The mixture was quenched with saturated NH4Cl and partitioned between water and ethyl acetate. The organic layer was separated, dried over MgSO4, filtered and concentrated to give 85 mg of the crude title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193227B2
Source datasetuspto-grants-2012_06
ORD IDord-1f8324259554487484ee94bb8f406dc8
Source noteuspto-grants-2012_06