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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499064Generated: October 30, 2026

4-Methylbenzoyl Chloride → HCID 178425840, compound

https://huagongshe.com/reaction/499064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantHCID 178428240HCID 178428240—
SolventPyridineHCID 1049—
ProductHCID 178425840HCID 17842584034%

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 p-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 (91 mg, 34%) as a white solid. 1H NMR: (400 MHz, DMSO) 1.99 (3H, brs), 2.33 (2H, qn), 2.40 (3H, s), 3.88 (4H, t), 5.38 (1H, brs), 5.59 (1H, vbrs), 7.36 (2H, d), 7.53 (2H, d), 7.87 (2H, d), 7.91 (2H, d), 9.20 (1H, brs), 10.36 (1H, s), 11.66 (1H, brs); MS (ES+) 472.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767672B2
Source datasetuspto-grants-2010_08
ORD IDord-007600d7f14242c2acf0bc60b6e34160
Source noteuspto-grants-2010_08