HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473992Generated: October 30, 2026
4-Methylbenzoyl Chloride → HCID 178425840, compound
https://huagongshe.com/reaction/473992
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Reactant | HCID 178428240 | HCID 178428240 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178425840 | HCID 178425840 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637511B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-4b2935426eb145be861a2c295585f8cd |
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| Source note | uspto-grants-2014_01 |
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