1-Aminopiperidin-4-OL → 5-(4-chlorophenyl)-6-(cyclopropylmethoxy)-N-(4-hydroxypiperidin-1-yl)-3-pyridinecarboxamide

HRID 240692Notes

Reaction equation

HRID 240692 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]([C:19]([OH:21])=O)[CH:11]=[N:12][C:13]=2[O:14][CH2:15][CH:16]2[CH2:18][CH2:17]2)=[CH:4][CH:3]=1.[NH2:22][N:23]1[CH2:28][CH2:27][CH:26]([OH:29])[CH2:25][CH2:24]1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:9]=[C:10]([C:19]([NH:22][N:23]3[CH2:28][CH2:27][CH:26]([OH:29])[CH2:25][CH2:24]3)=[O:21])[CH:11]=[N:12][C:13]=2[O:14][CH2:15][CH:16]2[CH2:17][CH2:18]2)=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 121256451-Aminopiperidin-4-OLHCID 666874825-(4-Chlorophenyl)-6-(cyclopropylmethoxy)nicotinic acid

Product 1

HCID 712943715-(4-chlorophenyl)-6-(cyclopropylmethoxy)-N-(4-hydroxypiperidin-1-yl)-3-pyridinecarboxamide

Procedure

The title compound was synthesized in analogy to Example 1 using 5-(4-chlorophenyl)-6-(cyclopropylmethoxy)-3-pyridinecarboxylic acid (CAN 1018782-76-7) and 1-amino-4-piperidinol (CAN 79414-82-7) as starting materials; MS (EI) 402.4 (M+H)+.

Sources & evidence

ORD record
ord-9e176afc87b34658aa32e50b739fc6ef
Source dataset
uspto-grants-2014_02
Patent number
US08648099B2

Reaction notes

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