Hydrochloric Acid → HCID 71268826, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:12]=[C:13]([NH:22][C:23]3[CH:42]=[CH:41][C:26]([CH2:27][N:28]4[CH2:33][CH2:32][N:31](C(OC(C)(C)C)=O)[CH2:30][CH2:29]4)=[CH:25][CH:24]=3)[C:14]3[C:19](=[O:20])[NH:18][N:17]=[CH:16][C:15]=3[N:21]=2)=[CH:7][CH:6]=1)=[O:4].[ClH:43]>O1CCOCC1>[ClH:43].[O:20]=[C:19]1[NH:18][N:17]=[CH:16][C:15]2[N:21]=[C:11]([C:8]3[CH:7]=[CH:6][C:5]([C:3]([O:2][CH3:1])=[O:4])=[CH:10][CH:9]=3)[N:12]=[C:13]([NH:22][C:23]3[CH:24]=[CH:25][C:26]([CH2:27][N:28]4[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]4)=[CH:41][CH:42]=3)[C:14]1=2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Tert-butyl 4-(4-(2-(4-(methoxycarbonyl)phenyl)-5-oxo-5,6-dihydropyrimido[4,5-d]pyridazin-4-ylamino)benzyl)piperazine-1-carboxylate (0.1 g, 0.175 mmol) was dissolved in dioxane.HCl (5 mL) and stirred at room temperature for 1.5 hours. The solid obtained was filtered and the residue washed with EtOAc and dried to give the desired product (40 mg).
Workup
- customThe solid obtained
- filtrationwas filtered
- washthe residue washed with EtOAc
- customdried
Sources & evidence
- ORD record
- ord-8aaf59ddb1b9416398f1e09f9a56650b
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09382277B2
Reaction notes
Loading…