Hydrochloride methanol → HCID 11848560, compound
Reaction equation
[N:1]1([C:8]2[CH:13]=[CH:12][N:11]=[C:10]([NH:14][CH:15]3[CH2:20][CH2:19][CH2:18][N:17]([CH:21]4[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]4)[CH:16]3[CH2:27][CH2:28][NH:29]C(=O)OC(C)(C)C)[N:9]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.CO>>[NH2:29][CH2:28][CH2:27][CH:16]1[CH:15]([NH:14][C:10]2[N:9]=[C:8]([N:1]3[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]3)[CH:13]=[CH:12][N:11]=2)[CH2:20][CH2:19][CH2:18][N:17]1[CH:21]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1Participants
3
Procedure
The compound 21 (102 mg) and 10% hydrogen chloride-methanol solution (2 mL) were stirred at room temperature for 5 hours. The reaction solution was concentrated, added aqueous 2N sodium hydroxide solution and then extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate, concentrated and obtained the title compound (71 mg) having the following physical properties.
Workup
- concentrationThe reaction solution was concentrated
- additionadded aqueous 2N sodium hydroxide solution
- extractionextracted with dichloromethane
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-00760a7f43d4492cb17b3602af8eb3de
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08680092B2
Reaction notes
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