2-Butyn-1-ol → HCID 23020169, compound
Reaction equation
Cl[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][N:3]=1.[CH2:13]([OH:17])[C:14]#[C:15][CH3:16]>>[CH2:13]([O:17][C:2]1[CH:12]=[CH:11][C:5]([C:6]([OH:8])=[O:7])=[CH:4][N:3]=1)[C:14]#[C:15][CH3:16]Participants
3
Procedure
The title compound was synthesized as described for Intermediate example I-92 in 38% yield starting from ethyl 6-chloronicotinate and 2-butyn-1-ol; 1H NMR (400 MHz, DMSO-d6) δ ppm 8.61-8.76 (m, 1 H), 8.03-8.23 (m, 1 H), 6.83-6.98 (m, 1 H), 4.94-5.05 (m, 2 H), 1.74-1.91 (m, 3 H); MS (ESI) m/z 192[M+H+], m/z 190[M−H+].
Sources & evidence
- ORD record
- ord-64db59f416f241e28bb0c8c2fb315142
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08143408B2
Reaction notes
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