Isonicotinic Acid → HCID 765384, compound
Reaction equation
[C:1]([OH:9])(=O)[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[I:10][C:11]1[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=1.C1C2C(=CC=CC=2)C=CC=1C(O)=O>>[I:10][C:11]1[CH:17]=[CH:16][C:14]([NH:15][C:1](=[O:9])[C:2]2[CH:3]=[CH:4][N:5]=[CH:6][CH:7]=2)=[CH:13][CH:12]=1Participants
4
Procedure
This compound was synthesized by the same procedure as for Example 15, except isonicotinic acid and 4-iodoaniline were used instead of 2-napthoic acid and 4-iodoaniline. M+325.1, mp 245-250° C.
Sources & evidence
- ORD record
- ord-d7eb3e8f4f524e59801808d0d5378779
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06780883B2
Reaction notes
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