HCID 14297705, compound → HCID 54095380, compound
Reaction equation
[F:1][C@@H:2]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[CH2:3][O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1.O[C:21]1[CH:26]=[CH:25][C:24]([C:27]2[N:32]=[CH:31][C:30]([CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])=[CH:29][N:28]=2)=[CH:23][CH:22]=1>>[CH2:33]([C:30]1[CH:29]=[N:28][C:27]([C:24]2[CH:25]=[CH:26][C:21]([O:10][C:9](=[O:11])[C:8]3[CH:12]=[CH:13][C:5]([O:4][CH2:3][C@@H:2]([F:1])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[CH:6][CH:7]=3)=[CH:22][CH:23]=2)=[N:32][CH:31]=1)[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41]Participants
3
Procedure
(S)-4-(2-Fluorooctyloxy)benzoic acid and 2-(4-hydroxyphenyl)-5-n-nonylpyrimidine are reacted analogously to give (S)-[4-(5-n-nonylpyrimidin-2-yl)phenyl]4-(2-fluorooctyloxy)benzoate.
Sources & evidence
- ORD record
- ord-cc16b688f9b64870ae3ba2814fd9e545
- Source dataset
- uspto-grants-1995_02
- Patent number
- US05393459
Reaction notes
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