HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235269Generated: October 31, 2026
N-Methylformanilide → HCID 23353992, compound
https://huagongshe.com/reaction/235269
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylformanilide | HCID 66737 | — |
| Reactant | HCID 10782547 | HCID 10782547 | — |
| Solvent | Chlorine monoxide | HCID 24646 | — |
| Product | HCID 23353992 | HCID 23353992 | 46.1% |
Reaction Steps
A mixture of 0.45 g of N-methylformanilide in 0.33 ml of phosphrus oxychloride was stirred at room temperature for an hour and 0.5 g of 2-(4 -chlorophenyl)-2,5,6,7-tetrahydro-3H-thieno-[2',3':6,7]cyclohepta[1,2-c]pyridazin-3-one was added thereto. After stirring at room temperature for 2 hours, the mixture was poured into ice-cold water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was chromatographed on a silica gel (SiO2 :40 g) column using chloroform as an eluent. The resulting solid was recrystallized from a mixed solvent of chloroform and ethanol to give 0.25 g of 2-(4-chlorophenyl)-9-formyl-2,5,6,7-tetrahydro-3H-thieno-[2',3':6,7]-cyclohepta[1,2-c]pyridazin-3-one as a pale yellow powder, melting at 170°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597918 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-ffef500251f94e9dae2e141c05282046 |
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| Source note | uspto-grants-1997_01 |
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