2-Aminophenol → HCID 69100358, compound

HRID 2115031Notes

Reaction equation

HRID 2115031 reaction equation
[CH2:1]([CH:8]1[CH2:13][CH2:12][N:11]([C:14](=[O:18])[C:15]([OH:17])=O)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[OH:26]>CCCCCC>[CH2:1]([CH:8]1[CH2:9][CH2:10][N:11]([C:14](=[O:18])[C:15]([NH:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[OH:26])=[O:17])[CH2:12][CH2:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 2

HCID 58012-AminophenolHCID 16110264(4-Benzylpiperidin-1-yl)oxoacetic acid

Product 1

HCID 69100358HCID 69100358, compound

Reagents, catalysts & solvents 1

HCID 8058HexaneSolvent

Procedure

The title compound is prepared from (4-benzyl-piperidin-1-yl)-oxo-acetic acid (Example 5b) and 2-aminophenol (Aldrich) according to the method described in Example 1c. Melting Point: 121-125-165° C. (hexane)

Sources & evidence

ORD record
ord-201c953c260e403da0c2db793fae229c
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

Loading…