Hydrochloric Acid → HCID 22340319, compound
Reaction equation
[ClH:1].[Cl:2][CH2:3][C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9]([NH:14]C(=O)C)[CH:10]=2)[N:5]=1.Cl>>[ClH:2].[ClH:1].[Cl:2][CH2:3][C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9]([NH2:14])[CH:10]=2)[N:5]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
To the N-[2-(chloromethyl)-6-quinolinyl]acetamide hydrochloride (900 mg, 3.32 mmol) obtained in Reference Example 6 was added 5N hydrochloric acid (17 ml), and the mixture was stirred at 100° C. for 2 hours. The reaction solution was concentrated under reduced pressure, and the resulting residue was washed with tetrahydrofuran to obtain the titled compound (849 mg) as powders.
Workup
- concentrationThe reaction solution was concentrated under reduced pressure
- washthe resulting residue was washed with tetrahydrofuran
Sources & evidence
- ORD record
- ord-7e9601225fc44cf2886c0c71f3a0d6c6
- Source dataset
- uspto-grants-2005_08
- Patent number
- US06930185B2
Reaction notes
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