HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235263Generated: October 29, 2026
N-Methylformanilide → HCID 23354006, compound
https://huagongshe.com/reaction/235263
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylformanilide | HCID 66737 | — |
| Reactant | HCID 10495037 | HCID 10495037 | — |
| Solvent | Chlorine monoxide | HCID 24646 | — |
| Product | HCID 23354006 | HCID 23354006 | 59.4% |
Reaction Steps
A mixture of 4.7 g of N-methylformanilide in 3.3 ml of phosphrus oxychloride was stirred at room temperature for an hour and 5.4 g of 2-(4-methylphenyl)-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 chloroform. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was chromatographed on a silica gel column using a mixed solvent of hexane and ethyl acetate (2:1) as an eluent. The solid was recrystallized from a mixed solvent of ethanol and ethyl acetate to give 3.5 g of 9-formyl-2-(4-methylphenyl)-2,5,6,7-tetrahydro-3H-thieno-[2',3':6,7]cyclohepta[1,2-c]pyridazin-3-one as a pale brown powder, melting at 127°-129° 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-2e0272fa8db241a0a24d3b733a26245d |
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| Source note | uspto-grants-1997_01 |
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