HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910468Generated: November 2, 2026
Phenylacetyl chloride → N-(6-chloropyridazin-3-yl)-2-phenylacetamide
https://huagongshe.com/reaction/1910468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | 6-Amino-3-chloropyridazine | HCID 21643 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-(6-chloropyridazin-3-yl)-2-phenylacetamide | HCID 86687867 | 88.3% |
Reaction Steps
To a solution of 3-amino-6-chloropyridazine (11.14 g, 86.0 mmol) in NMP (279 mL) at 19° C. was added phenylacetyl chloride (18.2 mL, 137.6 mmol) dropwise over 5 minutes with the internal temperature of the solution maintained Ti≦28° C. The resulting mixture was stirred at 19° C. for 90 minutes and poured into ice water (557 mL). The white precipitate was collected by suction filtration, rinsed with water (2×110 mL) and diethyl ether (110 mL). The product was dried overnight under high vacuum to afford N-(6-chloropyridazin-3-yl)-2-phenylacetamide (xxx, 18.8 g). 1H NMR (300 MHz, DMSO-d6) δ 11.57 (s, 1H), 8.40 (d, J=9.636 Hz, 1H), 7.90 (d, J=9.516 Hz, 1H), 7.36 (m, 5H) 3.82 (s, 2H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604016B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-0e1ed8361f3d4d0b9ce027a241117ba1 |
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| Source note | uspto-grants-2013_12 |
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