HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192396Generated: November 1, 2026
Chloroacetyl chloride → 2-Chloro-N-(6-methyl-pyrimidin-4-yl)-acetamide
https://huagongshe.com/reaction/2192396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 6-Methylpyrimidin-4-amine | HCID 572852 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Chloro-N-(6-methyl-pyrimidin-4-yl)-acetamide | HCID 67311001 | — |
Reaction Steps
6-Methyl-pyrimidin-4-yl amine (545 mg) was suspended in DCE (5 mL) and chloroacetylchloride (0.4 mL) was added dropwise. The reaction was heated in a microwave at 80° C. for 5 mins. The reaction mixture was cooled, filtered and a solid obtained. The reaction was repeated a second time and both batches of solid were combined, washed with dichloromethane then suspended in dichloromethane and sat. NaHCO3 (aq.) was added. The organic phase was collected and the aqueous layer extracted with dichloromethane (×2). The combined organic layer was dried over sodium sulphate and concentrated. The crude product was purified by silica gel chromatography eluting with 0-10% MeOH/dichloromethane to give the sub-titled compound as a yellow solid (120 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329729B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-1eb3fa1fdb7f40f680bbcd6ed7731817 |
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| Source note | uspto-grants-2012_12 |
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