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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031820Generated: October 31, 2026

Triethylamine → HCID 10372347, compound

https://huagongshe.com/reaction/1031820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantBenzyl octahydrocyclopenta[b]pyrrole-2-carboxylate--hydrogen chloride (1/1)HCID 13216857—
ReactantHCID 18631457HCID 18631457—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 10372347HCID 1037234737.3%

Reaction Steps

In 10 ml of N,N-dimethylformamide are dissolved 0.56 g of benzyl (S,S,S)-2-azabicyclo[3,3,0]octane-3-carboxylate.hydrochloride and 0.5 g of N-[(S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl]-L-alanine.hydrochloride, and 0.3 g of triethylamine is added to the solution under ice-cooling with stirring, followed by addition of 0.5 ml of diethyl phosphorocyanidate. After stirring for 30 minutes, there is added to the mixture 0.1 g of triethylamine, followed by stirring for 30 minutes and at room temperature for 1 hour. The reaction mixture is diluted with 100 ml of water and extracted with 100 ml of ethyl acetate. The extract is washed with 5% aqueous phosphoric acid and water, successively, and dried over anhydrous magnesium sulfate. The solvent is distilled off under reduced pressure, and the residue is purified by silica gel column chromatography (hexane:acetone=3:1) to give 0.26 g of benzyl (S,S,S)-2-[N-[(S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl]-L-alanyl]-2-azabicyclo[3,3,0]octane-3-carboxylate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954625
Source datasetuspto-grants-1990_09
ORD IDord-3d00aa0a3e8c4be3b7aacaa9480581b0
Source noteuspto-grants-1990_09