Hydrochloric Acid → HCID 178441357, compound
Reaction equation
[NH:1]1[CH:5]=[C:4]([CH2:6][CH2:7]/[CH:8]=[CH:9]/C(N)CC2CCCCC2)[N:3]=[CH:2]1.[ClH:19].C(C1N=CNC=1)CC#C>>[ClH:19].[CH2:6]([C:4]1[N:3]=[CH:2][NH:1][CH:5]=1)[CH2:7][C:8]#[CH:9]Participants
4
Procedure
4-But-3-ynylimidazole HCl was prepared from the deprotection of compound 26 by treatment with 2N HCl. ##STR76## 4-But-3-ynylimidazole (45) 1H-NMR (300 MHz, CD3OD): δ8.90 (s, 1H), 7.40 (s, 1H), 2.95 (t, J=6.9 Hz, 2H), 2.60 (dt, J=2.4 and 6.9 Hz, 2H), 2.40 (t, J=2.7 Hz, 1H); Mass Spectrum (Cl) m/e 121 (M+1).
Sources & evidence
- ORD record
- ord-3376a3405cf248b88dde43f75418af3f
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06166060
Reaction notes
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