Hydrochloric Acid → HCID 18538839, compound
Reaction equation
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]([N:12]([C:30]2[CH:35]=[CH:34][C:33]([Cl:36])=[C:32]([Cl:37])[CH:31]=2)[CH2:13][CH2:14][CH2:15][N:16]2[CH2:21][CH2:20][CH:19]([CH2:22][C:23]3[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=3)[CH2:18][CH2:17]2)=[O:11])[CH2:6][CH2:5]1)(=[O:3])[CH3:2].Cl>CO.C(OCC)(=O)C>[ClH:36].[C:1]([N:4]1[CH2:5][CH2:6][CH:7]([C:10]([N:12]([C:30]2[CH:35]=[CH:34][C:33]([Cl:36])=[C:32]([Cl:37])[CH:31]=2)[CH2:13][CH2:14][CH2:15][N:16]2[CH2:17][CH2:18][CH:19]([CH2:22][C:23]3[CH:24]=[CH:25][C:26]([F:29])=[CH:27][CH:28]=3)[CH2:20][CH2:21]2)=[O:11])[CH2:8][CH2:9]1)(=[O:3])[CH3:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The title compound of example 17 (1096 mg) dissolved in methanol was treated with 4N hydrogen chloride solution in ethyl acetate (0.75 mL) and the solvent was removed under reduced pressure. Diethyl ether was added to the residue, the resulting precipitate was collected by filtration, washed with diethyl ether, and dried under reduced pressure to afford the title compound (1060 mg) as a white amorphous solid.
Workup
- customthe solvent was removed under reduced pressure
- additionDiethyl ether was added to the residue
- filtrationthe resulting precipitate was collected by filtration
- washwashed with diethyl ether
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-5b78fb1d372a45e281096af6308da24f
- Source dataset
- uspto-grants-2003_05
- Patent number
- US06562978B1
Reaction notes
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