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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171527Generated: November 2, 2026

Methanol → Benzyl (s)-1-((1s,2r,4r/s)-4-(tert-butylamino)-2-propylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/1171527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTert-ButylamineHCID 6385—
ReactantSodium borohydrideHCID 4311764—
Reactantbenzyl (S)-2-oxo-1-((1S,2R)-4-oxo-2-propylcyclohexyl)pyrrolidin-3-ylcarbamateHCID 86596864—
CatalystHCID 178460666HCID 178460666—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
ProductBenzyl (s)-1-((1s,2r,4r/s)-4-(tert-butylamino)-2-propylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamateHCID 90985767—

Reaction Conditions

Temperature0 °C

Reaction Steps

A sample of benzyl (S)-2-oxo-1-((1S,2R)-4-oxo-2-propylcyclohexyl)pyrrolidin-3-ylcarbamate (114 mg) was dissolved in Ti(OiPr)4 (1.5 mL, 5.0 mmol) and tert-butylamine (0.14 mL, 1.8 mmol). The resultant solution was stirred at RT for 3 h before being cooled to 0° C. and charged successively with MeOH (2 mL) and NaBH4 (22.8 mg, 0.6 mmol). The mixture was stirred for 90 min while the solution slowly warmed to RT. The solution was diluted with methylene chloride (10 mL) and 0.5 N NaOH was added. The resultant suspension was filtered through a pad of Celite with EtOAc washings and the filtrate was dried, filtered, and concentrated in vacuo to afford benzyl (S)-1-((1S,2R,4R/S)-4-(tert-butylamino)-2-propylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamate as an inseparable mixture of diastereomers. MS found: (M+H)+=430.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-11c9bceb83b642e9b44720682e86e2ef
Source noteuspto-grants-2010_11