Hydrochloric Acid → HCID 68971896, compound
Reaction equation
C(OC(=O)[N:7]([CH2:23][CH2:24][C:25]([N:27]1[CH2:33][CH2:32][C:31]2[CH:34]=[C:35]([O:40][CH3:41])[C:36]([O:38][CH3:39])=[CH:37][C:30]=2[CH2:29][CH2:28]1)=[O:26])[CH2:8][CH:9]1[CH2:16][C:15]2[C:10]1=[CH:11][CH:12]=[C:13]([O:17][CH2:18][C:19]([NH:21][CH3:22])=[O:20])[CH:14]=2)(C)(C)C.[ClH:43]>C(O)C>[ClH:43].[CH3:39][O:38][C:36]1[C:35]([O:40][CH3:41])=[CH:34][C:31]2[CH2:32][CH2:33][N:27]([C:25](=[O:26])[CH2:24][CH2:23][NH:7][CH2:8][CH:9]3[CH2:16][C:15]4[C:10]3=[CH:11][CH:12]=[C:13]([O:17][CH2:18][C:19]([NH:21][CH3:22])=[O:20])[CH:14]=4)[CH2:28][CH2:29][C:30]=2[CH:37]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
At ambient temperature, 2.63 g (4.5 mmol) of the compound obtained in Step B above are mixed into 120 mL of ethanol together with 25 mL of 3.7N ethanolic HCl. After stirring for 1 day at ambient temperature, the solid formed is filtered off, rinsed with ethanol and with ether and dried in vacuo to obtain the desired compound in the form of the hydrochloride.
Workup
- customthe solid formed
- filtrationis filtered off
- washrinsed with ethanol and with ether
- customdried in vacuo
Sources & evidence
- ORD record
- ord-982fd8e1943e4a67a031f63e08e64fcc
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08076325B2
Reaction notes
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