Piperidine → Piperidin-1-yl-[5-(3-piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridin-2-yl]-methanone

HRID 1437688Notes

Reaction equation

HRID 1437688 reaction equation
Cl.[N:2]1([CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:13]=[C:14]3[CH:20]=[C:19]([C:21]([OH:23])=O)[NH:18][C:15]3=[N:16][CH:17]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.[NH:24]1[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1>>[N:24]1([C:21]([C:19]2[NH:18][C:15]3=[N:16][CH:17]=[C:12]([O:11][CH2:10][CH2:9][CH2:8][N:2]4[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]4)[CH:13]=[C:14]3[CH:20]=2)=[O:23])[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 684243705-(3-Piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic Acid Hydrochloride

Product 1

HCID 16727317Piperidin-1-yl-[5-(3-piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridin-2-yl]-methanoneYield 75%

Procedure

The title compound was synthesized in analogy to example 1 from 5-(3-piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid hydrochloride and piperidine to give the desired product as a light brown solid (75%).

Sources & evidence

ORD record
ord-7859769cda054c3eb610a36469b6479c
Source dataset
uspto-grants-2009_11
Patent number
US07622466B2

Reaction notes

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