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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088614Generated: October 26, 2026

Triethylamine → HCID 178444654, compound

https://huagongshe.com/reaction/1088614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 14671722HCID 14671722—
ReactantHCID 178454169HCID 178454169—
SolventDimethylformamideHCID 6228—
ProductHCID 178444654HCID 17844465463.9%

Reaction Steps

To a solution of N-t-butoxycarbonyl-L-histidine (363 mg) and 2(S)-amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (294 mg) in dry N,N-dimethylformamide (30 ml) which was cooled to 0° C., were added a solution of diphenyl phosphorylazide (390 mg) in dry N,N-dimethylformamide (5 ml)and triethylamine (144 mg). The mixture was stirred overnight at ambient temperature. After evaporation of the solvent, the residue was dissolved in ethyl acetate (30 ml) and the solution was washed with 10% citric acid solution, saturated sodium bicarbonate solution and water successively, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (chloroform as eluent) to give 2(S)-(N-t-butoxycarbonyl-L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (384 mg) as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963530
Source datasetuspto-grants-1990_10
ORD IDord-8933efa28b4d43e8b3007c54577d1695
Source noteuspto-grants-1990_10