Hydrochloric Acid → HCID 86761736, compound
Reaction equation
[OH-].[Li+].[CH:3]1([O:8][C:9]2[C:14]([O:15][CH3:16])=[CH:13][CH:12]=[CH:11][C:10]=2/[CH:17]=[CH:18]/[C:19]2[N:23]([C:24]3[N:29]=[N:28][C:27]([C:30]([O:32]CC)=[O:31])=[CH:26][CH:25]=3)[C:22]3[CH:35]=[CH:36][CH:37]=[CH:38][C:21]=3[N:20]=2)[CH2:7][CH2:6][CH2:5][CH2:4]1.Cl>C(O)C>[CH:3]1([O:8][C:9]2[C:14]([O:15][CH3:16])=[CH:13][CH:12]=[CH:11][C:10]=2/[CH:17]=[CH:18]/[C:19]2[N:23]([C:24]3[N:29]=[N:28][C:27]([C:30]([OH:32])=[O:31])=[CH:26][CH:25]=3)[C:22]3[CH:35]=[CH:36][CH:37]=[CH:38][C:21]=3[N:20]=2)[CH2:4][CH2:5][CH2:6][CH2:7]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
This compound was prepared by adding aqueous solution of lithium hydroxide (35 mg, 0.826 mmol) to a stirred solution of Example 19 that is Ethyl 6-{2-[(E)-2-(2-[Cyclopentyloxy]-3-methoxyphenyl)vinyl]-1H-benzimidazol-1-yl}pyridazine-3-carboxylate (200 mg, 0.413 mmol) in ethanol (5 ml) and stirring the reaction mixture at room temperature for 2 h. After completion of reaction the reaction mixture was acidified with 10% HCl until pH 4 was reached and at this pH the product precipitated out as a yellow solid which was filtered, washed with diethylether and dried under vaccum to get 210 mg of off-white solid.
Workup
- customThis compound was prepared
- customAfter completion of reaction the reaction mixture
- customprecipitated out as a yellow solid which
- filtrationwas filtered
- washwashed with diethylether
- customdried under vaccum
Sources & evidence
- ORD record
- ord-5177cee4ef574dccb3bd2a45d008d9dc
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08344010B2
Reaction notes
Loading…