4,5,6,7-Tetrahydro-1H-pyrrolo[3,2-C]pyridine → HCID 24899498, compound

HRID 550676Notes

Reaction equation

HRID 550676 reaction equation
[Cl:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11]([OH:13])=O)[CH:10]=2)[CH:7]=1.[NH:14]1[C:22]2[CH2:21][CH2:20][NH:19][CH2:18][C:17]=2[CH:16]=[CH:15]1>>[Cl:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11]([N:19]3[CH2:20][CH2:21][C:22]4[NH:14][CH:15]=[CH:16][C:17]=4[CH2:18]3)=[O:13])[CH:10]=2)[CH:7]=1

Participants

3

Reactant 2

HCID 214982824,5,6,7-Tetrahydro-1H-pyrrolo[3,2-C]pyridineHCID 336956786-Chloropyrazolo[1,5-A]pyrimidine-2-carboxylic acid

Product 1

HCID 24899498HCID 24899498, compound

Procedure

In close analogy to the procedure described in Example 1, 6-chloro-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid is reacted with 4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine to provide the title compound in moderate yield.

Sources & evidence

ORD record
ord-1405784211ea40e3b16e1f372eab6cbb
Source dataset
uspto-grants-2011_05
Patent number
US07947689B2

Reaction notes

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