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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282960Generated: November 1, 2026

Ammonia → N-[(Benzyloxy)carbonyl]-L-isoleucyl-L-prolyl-L-prolinamide

https://huagongshe.com/reaction/1282960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-[(Benzyloxy)carbonyl]-L-isoleucyl-L-prolyl-L-prolineHCID 54515815—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductN-[(Benzyloxy)carbonyl]-L-isoleucyl-L-prolyl-L-prolinamideHCID 53756909—

Reaction Steps

Benzyloxycarbonyl-isoleucyl-prolyl-proline (4.5 g) is dissolved in a mixture of tetrahydrofuran (30 ml) and triethylamine (1.4 ml). The solution is chilled in a -5° cooling bath and isobutyl chloroformate (1.6 ml) is added. The solution is allowed to warm to room temperature (10 minutes) and concentrated aqueous ammonia (10 ml) is added. After four hours stirring at room temperature, the reaction is concentrated in vacuo, diluted with ethyl acetate and washed sequentially with saturated sodium bicarbonate, water, 0.1 N hydrochloric acid and water. The organic phase is dried over magnesium sulfate and concentrated to dryness in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03973006
Source datasetuspto-grants-1976_08
ORD IDord-ba999c62b81b408e83dcc33283325721
Source noteuspto-grants-1976_08