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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655903Generated: November 3, 2026

Methyl chloroformate → HCID 19789645, compound

https://huagongshe.com/reaction/1655903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantButylamineHCID 8007—
ReactantTriethylamineHCID 8471—
Reactant4H-Pyrido(1,2-a)pyrimidine-3-carboxylic acid, 6-methyl-4-oxo-HCID 208416—
SolventChloroformHCID 6212—
ProductHCID 19789645HCID 1978964575.9%

Reaction Steps

A mixture containing i6.32 g (0.08 mol) of 6-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid and 12.4 ml (0.088 mol) of triethylamine in 480 ml of chloroform is cooled below -10° C. by ice-salt. A solution of 6.5 ml (0.08 mol) of methyl chloroformate in 40 ml of chloroform is dropped to the above mixture at a temperature between -12° C. and -15° C. during 15 minutes. After stirring for 5 minutes, 6.43 g (0.088 mol) of butylamine dissolved in 80 ml of chloroform are dropped to the above solution at a temperature between -10° C. and -15° C. during 50 minutes. The reaction mixture is stirred for 1 hour at the same temperature and then let to stand under cooling by ice. For working up, the mixture is washed 3 times with 150 ml of 5% sodium hydrogen carbonate solution each and then 3 times with 150 ml of water each. The organic phase is dried over anhydrous sodium sulfate and evaporated to give 14.9 g (71.8%) of the named product as yellow crystals, m.p.: 127°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252572
Source datasetuspto-grants-1993_10
ORD IDord-7aa8135c64604838a084d06ae844b0c7
Source noteuspto-grants-1993_10