RS 14203 → 6-(4-Pyridylmethyl)-8-(3-nitrophenyl)pyrido[2,3-d]pyridazin-5-one hydrochloride
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][N:8]2[C:13](=[O:14])[C:12]3[CH:15]=[CH:16][CH:17]=[N:18][C:11]=3[C:10]([C:19]3[CH:24]=[CH:23][CH:22]=[C:21]([N+:25]([O-:27])=[O:26])[CH:20]=3)=[N:9]2)=[CH:3][CH:2]=1.[ClH:28].CO>CO>[ClH:28].[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][N:8]2[C:13](=[O:14])[C:12]3[CH:15]=[CH:16][CH:17]=[N:18][C:11]=3[C:10]([C:19]3[CH:24]=[CH:23][CH:22]=[C:21]([N+:25]([O-:27])=[O:26])[CH:20]=3)=[N:9]2)=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 6-(4-pyridylmethyl)-8-(3-nitrophenyl)pyrido[2,3-d]pyridazin-5-one in methanol is added 5% HCl/MeOH in a dropwise manner with stirring until a clear solution is obtained. The solvent is stripped off. The resulting solid is triturated with ethyl ether. The product is filtered off and dried under vacuum yielding 6-(4-pyridylmethyl)-8-(3-nitrophenyl)pyrido[2,3-d]pyridazin-5-one hydrochloride.
Workup
- customis obtained
- customThe resulting solid is triturated with ethyl ether
- filtrationThe product is filtered off
- customdried under vacuum
Sources & evidence
- ORD record
- ord-cde025d4d2fa43d495d8c216eeeae18d
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05716954
Reaction notes
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