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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732707Generated: October 30, 2026

Triethylamine → HCID 178501235, compound

https://huagongshe.com/reaction/732707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactanttert-butyl [(1R)-1-(1-naphthyl)ethyl]{[(3R,4S)-4-phenylpyrrolidin-3-yl]methyl}carbamateHCID 86628525—
ReactantHCID 178501163HCID 178501163—
SolventTolueneHCID 1140—
ProductHCID 178501235HCID 17850123571%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 144 mg of trans-1,4-cyclohexanedicarboxylic acid monomethyl ester, 213 mg of DPPA and 6 ml of toluene was mixed with 157 mg of triethylamine at room temperature and stirred at 80° C. for 3Hours. The reaction solution was spontaneously cooled down to room temperature, and a 2 ml toluene solution of 332 mg of tert-butyl [(1R)-1-(1-naphthyl)ethyl]{[(3R,4S)-4-phenylpyrrolidin-3-yl]methyl}carbamate was added thereto and stirred overnight at room temperature. The reaction solution was washed with 1 M hydrochloric acid, water and 1 M sodium hydroxide aqueous solution in that order and dried with anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure, and the residue was purified by a silica gel column chromatography (chloroform-methanol) to obtain 336 mg of methyl trans-4-({[(3R,4S)-3-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]carbonyl}amino)cyclohexane-carboxylate as a colorless amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585886B2
Source datasetuspto-grants-2009_09
ORD IDord-8cf9da949fca424294c8a833a8c3b451
Source noteuspto-grants-2009_09