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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162157Generated: November 3, 2026

3-Methylbenzoyl chloride → HCID 178425290, compound

https://huagongshe.com/reaction/1162157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylbenzoyl chlorideHCID 74375—
ReactantHCID 178428240HCID 178428240—
SolventPyridineHCID 1049—
ProductHCID 178425290HCID 17842529033.1%

Reaction Steps

2-(4-Aminophenylthio)-6-(azetidin-1-yl)-N-(3-methyl-1H-pyrazol-5-yl)pyrimidin-4-amine (200 mg, 0.57 mmol) was taken up in pyridine (2 mL) and m-toluoyl chloride (0.187 mL, 1.42 mmol) was added dropwise at room temperature. After 15 minutes the reaction mixture was concentrated in vacuo and the residue taken up in methanol (3 mL). Sodium methoxide (25% w/w solution in MeOH, 1 mL) was added and the resulting cloudy solution stirred at room temperature for 15 minutes. The reaction mixture was purified directly by chromatography (silica, 5-100% EtOAc-petrol gradient elution) to give the title compound (89 mg, 33%) as a white solid. 1H NMR: (400 MHz, DMSO) 1.99 (3H, brs), 2.31 (2H, qn), 2.42 (3H, s), 3.88 (4H, t), 5.39 (1H, brs), 5.67 (1H, vbrs), 7.43-7.46 (2H, m), 7.54 (2H, d), 7.73-7.76 (2H, m), 7.91 (2H, d), 9.23 (1H, brs), 10.42 (1H, s), 11.67 (1H, brs). ES+472.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820685B2
Source datasetuspto-grants-2010_10
ORD IDord-79af1109e3ec45b3b0353f22533e7271
Source noteuspto-grants-2010_10