Hydrochloric Acid → HCID 11591930, compound
Reaction equation
C[O:2][C:3](=[O:40])[CH2:4][CH2:5][N:6]([CH2:29][CH2:30][CH2:31][CH2:32][N:33]([CH2:37][CH2:38][CH3:39])[CH2:34][CH2:35][CH3:36])[CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][N:15]([CH2:23][C:24]2[NH:25][CH:26]=[CH:27][N:28]=2)[CH2:16][C:17]2[N:18]([CH3:22])[CH:19]=[CH:20][N:21]=2)=[CH:10][CH:9]=1.Cl>CO>[CH2:37]([N:33]([CH2:34][CH2:35][CH3:36])[CH2:32][CH2:31][CH2:30][CH2:29][N:6]([CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][N:15]([CH2:23][C:24]2[NH:25][CH:26]=[CH:27][N:28]=2)[CH2:16][C:17]2[N:18]([CH3:22])[CH:19]=[CH:20][N:21]=2)=[CH:10][CH:9]=1)[CH2:5][CH2:4][C:3]([OH:40])=[O:2])[CH2:38][CH3:39]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound (129 mg) obtained in Example 34-3 was dissolved in anhydrous methanol (1.0 ml) and added with concentrated hydrochloric acid (10.0 ml) and the whole was refluxed under heating. After completion of the reaction, the solvent was distilled off, thereby obtaining a hydrochloride (71.4 mg) of the subject compound as a pale-yellow solid.
Workup
- temperaturethe whole was refluxed
- temperatureunder heating
- customAfter completion of the reaction
- distillationthe solvent was distilled off
Sources & evidence
- ORD record
- ord-748a4b1eb84a4507a4588d6f7c9a456a
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07932281B2
Reaction notes
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