Hydrochloric Acid → HCID 178479713, compound
Reaction equation
C(OC([N:8]1[CH2:12][CH2:11][CH2:10][C@H:9]1[C:13]1[NH:14][CH:15]=[C:16]([C:18]2[CH:23]=[CH:22][C:21]([CH:24]3[N:28]([C:29]4[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=4)[CH:27]([C:36]4[CH:41]=[CH:40][C:39]([NH:42][C:43]([C@@H:45]5[CH2:49][CH2:48][CH2:47][N:46]5C(OC(C)(C)C)=O)=[O:44])=[CH:38][CH:37]=4)[CH2:26][CH2:25]3)=[CH:20][CH:19]=2)[N:17]=1)=O)(C)(C)C.[ClH:57]>O1CCOCC1>[ClH:57].[F:35][C:32]1[CH:33]=[CH:34][C:29]([N:28]2[CH:24]([C:21]3[CH:20]=[CH:19][C:18]([C:16]4[N:17]=[C:13]([C@@H:9]5[CH2:10][CH2:11][CH2:12][NH:8]5)[NH:14][CH:15]=4)=[CH:23][CH:22]=3)[CH2:25][CH2:26][CH:27]2[C:36]2[CH:41]=[CH:40][C:39]([NH:42][C:43]([C@@H:45]3[CH2:49][CH2:48][CH2:47][NH:46]3)=[O:44])=[CH:38][CH:37]=2)=[CH:30][CH:31]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolved the product from Example 39H (350 mg, 0.458 mmol) in 4M hydrochloric acid in dioxane solution (6 mL) and stirred the solution at room temperature for 30 min then concentrated the mixture under high vacuum to a solid (approx. 310 mg) as a hydrochloride salt that was used directly in the next reaction.
Workup
- concentrationthen concentrated the mixture under high vacuum to a solid (approx. 310 mg) as a hydrochloride salt that
- customwas used directly in the next reaction
Sources & evidence
- ORD record
- ord-9f595549bce5423384b67eaba54bb5f1
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691938B2
Reaction notes
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