Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701152Generated: October 26, 2026

Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/1701152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBoc-gly-pro-OHHCID 11673468—
SolventTetrahydrofuranHCID 8028—
ProductN,N'-DicyclohexylureaHCID 4277—

Reaction Steps

A portion (10.3 g=0.05 mole) of dicyclohexylcarbodiimide (DCC) was added dropwise under stirring at 0° C. to a solution of N-Boc-glycyl-L-proline prepared in accordance with the method described in J. Chem. Soc. (C), 954 (1969) (27.2 g=0.1 mole) in dried THF (100 ml) and the reaction mixture was kept under continuous stirring for 45 minutes. To the filtrate obtained by filtering-off of dicyclohexyl urea precipitated in the mixture, was added at 0° C. a solution of 7-amino-4-methylcoumarin (8.75 g=0.05 mole) in dimethylformamide (DMF) (60 ml). After standing overnight at room temperature, the reaction mixture was concentrated in vacuo to give a residue which was dissolved in ethyl acetate (300ml.). The solution was washed successively with 1 N hydrochloric acid, aqueous 5% sodium bicarbonate and water, dried with anhydrous magnesium sulfate, and concentrated in vacuo. The residue was recrystalized from a binary mixture of ethyl acetate (150ml) and n-hexance (70ml) to give 20.1g (yield, 93.4%) of crystalline 7-(n-BOC-glycyl-L-prolyl)amino-4-methylcoumarin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191809
Source datasetuspto-grants-1980_03
ORD IDord-d05f46baf5ae48a9b0770180b7603ac2
Source noteuspto-grants-1980_03