N-Piperidinoethanol → HCID 68681197, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][NH:10][S:11]([C:14]1[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=1)(=[O:13])=[O:12].[N:21]1([CH2:27][CH2:28]O)[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1.FC1C=CC(OC2C=CC(S(N3CCC4C(=CC=C(OCCCN5CCN(C)CC5)C=4)C3C(OC)=O)(=O)=O)=CC=2)=CC=1>>[CH3:20][C:17]1[CH:16]=[CH:15][C:14]([S:11]([NH:10][CH2:9][CH2:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[O:1][CH2:28][CH2:27][N:21]2[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]2)(=[O:13])=[O:12])=[CH:19][CH:18]=1Participants
4
Procedure
N-[2-(2-Hydroxyphenyl)ethyl]-4-methylbenzenesulfonamide is reacted with 2-piperidin-1-ylethanol by the method described under 3C. Yield 69%.
Sources & evidence
- ORD record
- ord-a26df9867cf84c5486f69407e0d38e75
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858619B2
Reaction notes
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