Hydrochloric Acid → HCID 22478527, compound
Reaction equation
COC[O:4][C:5]1[CH:6]=[C:7]([N:11]2[CH2:17][CH2:16][CH2:15][NH:14][CH2:13][CH2:12]2)[CH:8]=[N:9][CH:10]=1.[ClH:18]>>[ClH:18].[OH:4][C:5]1[CH:6]=[C:7]([N:11]2[CH2:17][CH2:16][CH2:15][NH:14][CH2:13][CH2:12]2)[CH:8]=[N:9][CH:10]=1Participants
3
Procedure
1-(5-Methoxymethoxy-3-pyridyl)-homopiperazine (8.5 g, 35.9 mmol) was stirred in hydrochloric acid (4 M, 100 ml) at room temperature for 1 h. The excess of hydrochloric acid was evaporated. A crystaline compound was obtained by triturating with a mixture of 5% methanol and ether. Yield 9.56 g, 100%. Mp 290-300° C.
Workup
- customThe excess of hydrochloric acid was evaporated
- customA crystaline compound was obtained
- customby triturating with a mixture of 5% methanol and ether
Sources & evidence
- ORD record
- ord-144b3eab0e8f4f9d9fb1e11459f06150
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06825189B1
Reaction notes
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