4-Pyridinepropanol → HCID 54209077, compound
Reaction equation
[C:1]1([CH:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:8]([N:10]=[C:11]=[O:12])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26][CH2:27][OH:28])=[CH:21][CH:20]=1>>[N:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26][CH2:27][O:28][C:11](=[O:12])[NH:10][C:8](=[O:9])[CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:21][CH:20]=1Participants
3
Procedure
The title compound, brown solid, m.p. 147-50° C. and MS: m/e=374.4 (M+H+) was prepared in accordance with the general method of example 1 from diphenylacetyl isocyanate and 3-pyridin-4-yl-propan-1-ol.
Sources & evidence
- ORD record
- ord-837f3c753c514ddf9980e3f353e66bdb
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06596743B2
Reaction notes
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