Benzeneacetic acid, 4-hydroxy-, methyl ester → HCID 18670277, compound
Reaction equation
[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][CH:14]([OH:17])[CH2:13][CH2:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O[C:19]1[CH:24]=[CH:23][C:22]([CH2:25][C:26]([O:28][CH3:29])=[O:27])=[CH:21][CH:20]=1>>[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][CH:14]([O:17][C:19]2[CH:24]=[CH:23][C:22]([CH2:25][C:26]([O:28][CH3:29])=[O:27])=[CH:21][CH:20]=2)[CH2:13][CH2:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
1-(Benzyloxycarbonyl)piperidin-4-ol and methyl 4-hydroxyphenylacetate were treated in the same manner as the one of Production Example 65 to thereby give the title compound as a pale green powder.
Sources & evidence
- ORD record
- ord-529ff43e10e643da947dd3860106e062
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06518423B1
Reaction notes
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