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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280743Generated: October 31, 2026

Isopropylamine → Ethyl 4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/2280743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
Reactant4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
ReactantDiisopropylethylamineHCID 81531—
SolventEthanolHCID 702—
ProductEthyl 4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylateHCID 1049123792%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 4-chloro-2-(methylthio)pyrimidine-5-carboxylate (10 g, 43.0 mmol), propan-2-amine (4.21 mL, 49.4 mmol) and DIEA (9.76 mL, 55.9 mmol) in ethanol (140 mL) was heated at 60° C. overnight. After cooling to room temperature, the solvent was concentrated under reduced pressure and water was added. The aqueous phase was extracted three times with ethyl acetate and the combined organic phases were dried over magnesium sulfate, filtered and evaporated to give ethyl 4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxylate (10.10 g, 39.5 mmol, 92% yield) as a colorless oil. MS (ESI) m/z 256.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139534B2
Source datasetuspto-grants-2015_09
ORD IDord-0e95d47c47ca47e487020a94ad3682b3
Source noteuspto-grants-2015_09