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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903190Generated: November 2, 2026

Isobutyl chloroformate → HCID 13288203, compound

https://huagongshe.com/reaction/1903190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl chloroformateHCID 62365—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 12687390HCID 12687390—
ReactantHCID 12819307HCID 12819307—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 13288203HCID 13288203—

Reaction Steps

Into 400 ml of chloroform, were added 5 g of 6-(4-carboxybutoxy)-3,4-dihydrocarbostyril and 3.2 g of DBU. The outside of the reaction vessel containing the above mentioned mixture was ice-cooled and 2.8 g of isobutyl chloroformate was added dropwise to the mixture under stirring condition. After the addition operation, stirring was continued at a room temperature for 30 minutes and 3.9 g of N-(3-hydroxypropyl)-N-cyclohexylmethylamine was added to the reaction mixture and the reaction was continued for 3 hours. After the reaction was completed, the reaction mixture was washed with 1 N-NaOH aqueous solution, 10% HCl and water in this order and was dried with anhydrous Na2SO4. The drying agent was removed by filtration and the thus obtained dried product was concentrated to obtain a residue. The residue was treated by a silica-gel column chromatography (solvent used was a mixture of chloroform:methanol=40:1). The elute obtained was concentrated and was recrystallized from ethyl acetate-petroleum ether. 4.0 Grams of 6-{4-[N-cyclohexylmethyl-N-(3-hydroxypropyl)aminocarbonyl]butoxy}-3,4-dihydrocarbostyril was obtained in the form of colorless needle-like crystals. Melting point: 95°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435404
Source datasetuspto-grants-1984_03
ORD IDord-2552c8108baa40938179a0ec6cf9262c
Source noteuspto-grants-1984_03