3-Aminopyridine → HCID 69236764, compound

HRID 2219587Notes

Reaction equation

HRID 2219587 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:11](Br)=[CH:10][CH:9]=[C:8]([CH:13]2[CH2:15][CH2:14]2)[N:7]=1)=[O:5])[CH3:2].[NH2:16][C:17]1[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=1>[Pd]>[CH2:1]([O:3][C:4]([C:6]1[C:11]([NH:16][C:17]2[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=2)=[CH:10][CH:9]=[C:8]([CH:13]2[CH2:15][CH2:14]2)[N:7]=1)=[O:5])[CH3:2]

Participants

4

Reactant 2

HCID 100093-AminopyridineHCID 69235471Ethyl 3-bromo-6-cyclopropyl-2-pyridinecarboxylate

Product 1

HCID 69236764HCID 69236764, compound

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

Palladium catalysed arylation of 3-Bromo-6-cyclopropyl-pyridine-2-carboxylic acid ethyl ester with 3-Aminopyridine according to the general procedure described in example 78 step 3 yielded the title compound as a light yellow solid, MS (ISP): m/e=284.4 (M+H+).

Sources & evidence

ORD record
ord-3092602dba144d8b95f84aa8cef6f1f4
Source dataset
uspto-grants-2008_08
Patent number
US07414060B2

Reaction notes

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