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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696440Generated: October 31, 2026

(4-(Methylamino)-2-(methylthio)pyrimidin-5-yl)methanol → 4-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/1696440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(Methylamino)-2-(methylthio)pyrimidin-5-yl)methanolHCID 10679092—
CatalystManganese dioxideHCID 14801—
SolventChloroformHCID 6212—
Product4-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehydeHCID 1060752092%

Reaction Steps

A mixture of (4-(methylamino)-2-(methylthio)pyrimidin-5-yl)methanol (22.0 g, 119 mmol) and MnO2 (44 g, 714 mmol) in CHCl3 (300 mL) was stirred at RT for 3 h. The reaction was filtered and the filtrate concentrated to give 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carbaldehyde as a pale solid (20 g, 92% yield). 1H NMR (400 MHz, DMSO-d6): δ 9.71 (s, 1H), 8.60 (brs, 1H), 8.49 (s, 1H), 2.96 (d, J=4.8 Hz, 3H), 2.48 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163756B2
Source datasetuspto-grants-2012_04
ORD IDord-ea514eccca424e9f90bc5f9e3db8806c
Source noteuspto-grants-2012_04