1-Methyl-3-aminopyrazole → HCID 16118956, compound

HRID 1787611Notes

Reaction equation

HRID 1787611 reaction equation
Br[C:2]1[CH:11]=[N:10][C:9](Cl)=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.[N:13]1[CH:18]=[C:17](B(O)O)[CH:16]=[CH:15][CH:14]=1.[CH3:22][N:23]1[CH:27]=[CH:26][C:25]([NH2:28])=[N:24]1>>[CH3:22][N:23]1[CH:27]=[CH:26][C:25]([NH:28][C:9]2[N:10]=[CH:11][C:2]([C:15]3[CH:14]=[N:13][CH:18]=[CH:17][CH:16]=3)=[C:3]3[C:8]=2[N:7]=[CH:6][CH:5]=[CH:4]3)=[N:24]1

Participants

4

Reactant 3

HCID 1372541-Methyl-3-aminopyrazoleHCID 27343783-Pyridinylboronic acidHCID 422813655-Bromo-8-chloro-1,7-naphthyridine

Product 1

HCID 16118956HCID 16118956, compound

Procedure

The title compound, MS: m/e=303.2 (M+H+), was prepared in accordance with the general method of example 15 step 1 and step 3 from 5-bromo-8-chloro-[1,7]naphthyridine (Example H), 5-pyridineboronic acid and 1-methyl-1H-pyrazol-3-ylamine.

Sources & evidence

ORD record
ord-0740054aff2446f588012d2b2a5ba8cd
Source dataset
uspto-grants-2009_03
Patent number
US07511055B2

Reaction notes

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