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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336516Generated: October 27, 2026

4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester → Ethyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/336516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylateHCID 29569711.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Chloro-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester (10 g, 429 mmol) was dissolved in acetonitrile to which DIPEA (4.34 g, 642 mmol) and methylamine hydrochloride (11.10 g, 858 mmol) was added. The reaction mixture was stirred at 100° C. for 3 hours, then cooled to room temperature and poured in to ice water. Off-white crystalline solid precipitated out. The solid was collected by filtration on a Buchner funnel and dried under vacuum to give the desired product (11 g). 1H NMR (DMSO-d6): δ 1.30 (t, J=7 Hz, 3H), δ 2.46 (s, 3H), δ 2.99 (d, J=5 Hz, 3H), δ 4.29 (q, J=7 Hz, 2H), δ 8.09 (br, s, 1H), δ 8.53 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889696B2
Source datasetuspto-grants-2014_11
ORD IDord-a4b193244f334bc8b176808aa1d83f85
Source noteuspto-grants-2014_11