Hydrochloric Acid → HCID 68709452, compound
Reaction equation
[C:1]([NH:5][CH2:6][C:7](=[O:27])[CH2:8][CH2:9][N:10]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[N:12]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[S:11]1(=[O:26])=[O:25])([CH3:4])([CH3:3])[CH3:2].C(OC(=O)N)(C)(C)C.CO.[ClH:38]>C(OCC)C.O1CCOCC1>[ClH:38].[C:1]([NH:5][CH2:6][C:7](=[O:27])[CH2:8][CH2:9][N:10]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[N:12]([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[S:11]1(=[O:26])=[O:25])([CH3:4])([CH3:2])[CH3:3]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
The clear oil, 1-(tert-butylamino)-4-(2,2-dioxido-3-phenyl-2,1,3-benzothiadiazol-1(3H)-yl)butan-2-one-carbamic acid tert-butyl ester, was dissolved in diethyl ether and methanol and 4N HCl in dioxane was added a precipitate formed. The reaction was filtered to afford 12 mg of 1-(tert-butylamino)-4-(2,2-dioxido-3-phenyl-2,1,3-benzothiadiazol-1(3H)-yl)butan-2-one hydrochloride as a white solid.
Workup
- customformed
- filtrationThe reaction was filtered
Sources & evidence
- ORD record
- ord-7b3a132ce0eb4c5d9108d0f003149a40
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07601722B2
Reaction notes
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