Hydrochloric Acid → HCID 69288600, compound
Reaction equation
C(OC([NH:8][C@H:9]([CH2:29][C:30]1[CH:35]=[C:34]([F:36])[C:33]([F:37])=[CH:32][C:31]=1[F:38])[CH2:10][C:11]([N:13]1[CH2:19][CH2:18][CH2:17][N:16]([CH3:20])[C:15](=[O:21])[C@H:14]1[CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:12])=O)(C)(C)C.[ClH:39]>O1CCOCC1>[ClH:39].[NH2:8][C@H:9]([CH2:29][C:30]1[CH:35]=[C:34]([F:36])[C:33]([F:37])=[CH:32][C:31]=1[F:38])[CH2:10][C:11]([N:13]1[CH2:19][CH2:18][CH2:17][N:16]([CH3:20])[C:15](=[O:21])[C@H:14]1[CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound from Step C was dissolved in 4M hydrogen chloride in dioxane and evaporated after 2.5 h to yield the desired product.
Workup
- customevaporated after 2.5 h
Sources & evidence
- ORD record
- ord-2f1689cee2f14229a3eaafdca7c89015
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07101871B2
Reaction notes
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