6-Bromo-2-(pyrrolidin-1-YL)-[1,2,4]triazolo[1,5-A]pyridine → 2-Pyrrolidin-1-yl-[1,2,4]triazolo[1,5-a]pyridin-6-ylamine

HRID 588457

Reaction equation

HRID 588457 reaction equation
BrC1C=CC2N(N=C(N3CCCC3)N=2)C=1.[N:16]1([C:22]2[N:31]=[C:25]3[CH:26]=[CH:27][C:28]([NH2:30])=[CH:29][N:24]3[N:23]=2)[CH2:21][CH2:20]O[CH2:18][CH2:17]1>>[N:16]1([C:22]2[N:31]=[C:25]3[CH:26]=[CH:27][C:28]([NH2:30])=[CH:29][N:24]3[N:23]=2)[CH2:21][CH2:20][CH2:18][CH2:17]1

Participants

3

Reactant 2

HCID 717439856-Bromo-2-(pyrrolidin-1-YL)-[1,2,4]triazolo[1,5-A]pyridineHCID 894644042-Morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-6-amine

Product 1

HCID 894638012-Pyrrolidin-1-yl-[1,2,4]triazolo[1,5-a]pyridin-6-ylamine

Procedure

Using 6-Bromo-2-pyrrolidin-1-yl-[1,2,4]triazolo[1,5-a]pyridine, this compound was prepared following the same method as for the synthesis of 2-morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-6-ylamine. Brown solid (1.1 g, 81%). MS: m/z=204 (M+H+).

Workup

  1. customthis compound was prepared

Sources & evidence

ORD record
ord-a1da7ceab640474a93121c858b22fd97
Source dataset
uspto-grants-2016_01
Patent number
US09227970B2

Linked notes

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