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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246597Generated: October 31, 2026

Tert-Butylamine → 2-(trimethylsilyl)ethyl (1R,2S,5R)-2-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexylcarbamate

https://huagongshe.com/reaction/2246597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(trimethylsilyl)ethyl (1R,2S)-2-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-5-oxocyclohexylcarbamateHCID 86618158—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-(trimethylsilyl)ethyl (1R,2S,5R)-2-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexylcarbamateHCID 8661814083%

Reaction Steps

To a solution of 2-(trimethylsilyl)ethyl (1R,2S)-2-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-5-oxocyclohexylcarbamate (0.550 g, 1.123 mmol) in methylene chloride (0.4 mL) was added t-butylamine (1.180 ml, 11.23 mmol) and Titanium(IV) isopropoxide (6.63 ml, 22.47 mmol). This mixture was stirred for 2 h before sodium cyanoborohydride (127 mg, 2.022 mmol) and MeOH (1 mL) were added. After 2 h, methylene chloride (50 mL) was added, followed by 1N NaOH. The mixture was filtered through Celite to remove the titanium salts. The filtrate was dried and concentrated in vacuo to give 2-(trimethylsilyl)ethyl (1R,2S,5R)-2-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexylcarbamate and its 5S diastereomer as a mixture (510 mg, 0.933 mmol, 83% yield). LC/MS found [M+H]+=547.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687508B2
Source datasetuspto-grants-2010_03
ORD IDord-7ec92587c0914631a5a0427e4cb359d3
Source noteuspto-grants-2010_03