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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701748Generated: October 31, 2026

Methyl chloroformate → HCID 20483501, compound

https://huagongshe.com/reaction/1701748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantHCID 20483409HCID 20483409—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 20483501HCID 20483501—

Reaction Steps

5.4 ml of chloroformic acid methyl ester are added dropwise, whilst stirring, to 12.4 g of 5-(2'-aminoethyl)-2-(3'-isopropylamino-2'-hydroxy-propoxy)-pyridine, dissolved in a mixture of 45 ml of isopropanol and 45 ml of water, at a temperature of 20°-35° C., with cooling by means of ice water, if necessary. The reaction mixture is stirred further for one hour at room temperature and is evaporated in vacuo, and the evaporation residue is dissolved in approx. 30 ml of water. This solution is extracted with 20 ml of ethyl acetate and the acid aqueous phase is rendered alkaline with concentrated sodium hydroxide solution. The oil which precipitates is extracted with dichloromethane. After drying the solution over magnesium sulphate and evaporating off the solvent, 2-(3'-isopropylamino-2'-hydroxy-propoxy)-5-(2'-methoxycarbonylaminoethyl)-pyridine is obtained, melting at 97°-99° C. after recrystallisation from a little butanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04195090
Source datasetuspto-grants-1980_03
ORD IDord-1c3b0755278a47c987f3592704393f19
Source noteuspto-grants-1980_03