[6-(4-Fluorophenoxy)-2-pyridyl]methanol → HCID 53733807, compound

HRID 1413097Notes

Reaction equation

HRID 1413097 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][CH:10]([CH:14]([CH3:16])[CH3:15])[C:11]([OH:13])=[O:12])=[CH:4][CH:3]=1.[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([CH:24]=[CH:25][CH:26]([CH:30]([CH3:32])[CH3:31])[C:27]([OH:29])=[O:28])=[CH:20][CH:19]=1.[F:33][C:34]1[CH:48]=[CH:47][C:37]([O:38][C:39]2[N:44]=[C:43]([CH2:45]O)[CH:42]=[CH:41][CH:40]=2)=[CH:36][CH:35]=1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[CH:9][CH:10]([CH:14]([CH3:16])[CH3:15])[C:11]([O:13][CH2:45][C:43]2[CH:42]=[CH:41][CH:40]=[C:39]([O:38][C:37]3[CH:47]=[CH:48][C:34]([F:33])=[CH:35][CH:36]=3)[N:44]=2)=[O:12])=[CH:6][CH:7]=1.[Cl:17][C:18]1[CH:19]=[CH:20][C:21]([CH:24]=[CH:25][CH:26]([CH:30]([CH3:32])[CH3:31])[C:27]([O:29][CH2:45][C:43]2[CH:42]=[CH:41][CH:40]=[C:39]([O:38][C:37]3[CH:47]=[CH:48][C:34]([F:33])=[CH:35][CH:36]=3)[N:44]=2)=[O:28])=[CH:22][CH:23]=1

Participants

5

Reactant 3

HCID 20285867[6-(4-Fluorophenoxy)-2-pyridyl]methanolHCID 538855142-Isopropyl-4-(4-fluorophenyl)-3-butenoic acidHCID 54136759HCID 54136759, compound

Product 2

HCID 53733807HCID 53733807, compoundHCID 53989686HCID 53989686, compound

Procedure

By the procedure of Example 1, the acid chloride of each of 4-(4-fluorophenyl)-2-isopropyl-3-butenoic acid and 4-(4-chlorophenyl)-2-isopropyl-3-butenoic acid is reacted with [6-(4-fluorophenoxy)-2-pyridyl] methanol, yielding [6-(4-fluorophenoxy)-2-pyridyl]methyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate and [6-(4-fluorophenoxy)-2-pyridyl]methyl 4-(4-chlorophenyl)-2-isopropyl-3-butenoate, respectively.

Sources & evidence

ORD record
ord-18b82b52f3d24aa2905a1801f2caa4ef
Source dataset
uspto-grants-1981_02
Patent number
US04248875

Reaction notes

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