Hydrochloric Acid → HCID 12044599, compound
Reaction equation
[CH3:1][C:2]1([CH3:50])[C:6](=[O:7])[N:5]([C@@H:8]([CH2:25][CH:26]2[CH2:28][CH2:27]2)[C:9]([NH:11][CH:12]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=2)[CH2:13][C:14]([O:16]CC)=[O:15])=[O:10])[C:4](=[O:29])[N:3]1[CH2:30][C:31]1[CH:36]=[CH:35][C:34]([NH:37][C:38]([NH:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][C:42]=2[CH3:47])=[O:39])=[C:33]([O:48][CH3:49])[CH:32]=1.Cl>>[CH3:1][C:2]1([CH3:50])[C:6](=[O:7])[N:5]([C@@H:8]([CH2:25][CH:26]2[CH2:28][CH2:27]2)[C:9]([NH:11][CH:12]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=2)[CH2:13][C:14]([OH:16])=[O:15])=[O:10])[C:4](=[O:29])[N:3]1[CH2:30][C:31]1[CH:36]=[CH:35][C:34]([NH:37][C:38]([NH:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][C:42]=2[CH3:47])=[O:39])=[C:33]([O:48][CH3:49])[CH:32]=1Participants
3
Procedure
The compound was prepared analogously to Example 10 from 170 mg (0.248 mmol) of the compound of Example 15, but was not converted into the hydrochloride by addition of hydrochloric acid. Yield: 160 mg (98%).
Sources & evidence
- ORD record
- ord-686c517f84a34eac975335b48a390488
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06680333B2
Reaction notes
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