Hydrochloric Acid → HCID 131726507, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]3[C:14](=[CH:15][CH:16]=2)[C@@H:13]([C@H:17]([NH:26]C(=O)OC(C)(C)C)[C:18]([N:20]2[CH2:24][CH2:23][C@H:22]([F:25])[CH2:21]2)=[O:19])[CH2:12][CH2:11]3)=[CH:4][CH:3]=1.[ClH:34]>O1CCOCC1>[ClH:34].[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:9]=[C:10]3[C:14](=[CH:15][CH:16]=2)[C@@H:13]([C@H:17]([NH2:26])[C:18]([N:20]2[CH2:24][CH2:23][C@H:22]([F:25])[CH2:21]2)=[O:19])[CH2:12][CH2:11]3)=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 24.5 mg of the compound from Step H in 1 mL of 4N hydrogen chloride in dioxane was stirred at ambient temperature for 1 h and then concentrated. The resultant solid was washed with ether and dried in vacuo to give the title compound. Mass spectrum (MS): m/z 357 (M+1).
Workup
- concentrationconcentrated
- washThe resultant solid was washed with ether
- customdried in vacuo
Sources & evidence
- ORD record
- ord-e0444ef7af524a67aa48ad9b25f90497
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07238683B2
Reaction notes
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