Hydrochloric Acid → HCID 66763352, compound
Reaction equation
C(O[C:6](=O)[N:7]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C:15](=[O:38])[NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([CH2:23][NH:24][C:25]3[C:34]4[C:29](=[C:30]([C:35](=[O:37])[NH2:36])[CH:31]=[CH:32][CH:33]=4)[N:28]=[CH:27][N:26]=3)[CH:18]=2)[CH:10]=1)C)(C)(C)C.Cl>O1CCOCC1>[CH3:6][NH:7][C:9]1[CH:10]=[C:11]([CH:12]=[CH:13][CH:14]=1)[C:15]([NH:16][C:17]1[CH:18]=[C:19]([CH:20]=[CH:21][CH:22]=1)[CH2:23][NH:24][C:25]1[C:34]2[C:29](=[C:30]([C:35]([NH2:36])=[O:37])[CH:31]=[CH:32][CH:33]=2)[N:28]=[CH:27][N:26]=1)=[O:38]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
59 mg (0.11 mmol) (3-{3-[(8-Carbamoyl-quinazolin-4-ylamino)-methyl]-phenylcarbamoyl}-phenyl)-methyl-carbamic acid tert-butyl ester were dissolved in 3 ml dioxane and 560 μl 4 N HCl in dioxane were added. The mixture was stirred overnight, filtered and washed with dioxane.
Workup
- filtrationfiltered
- washwashed with dioxane
Sources & evidence
- ORD record
- ord-a2c43f2ab5944f06aad1387ac518e454
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040560B2
Reaction notes
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