3-Aminopyridine → HCID 68574330, compound

HRID 1949060Notes

Reaction equation

HRID 1949060 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7](Cl)[CH:8]=2)[N:3]=1.[CH3:13][C:14]1[O:18][C:17]([CH2:19][NH2:20])=[CH:16][CH:15]=1.[NH2:21][C:22]1[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=1>>[CH3:13][C:14]1[O:18][C:17]([CH2:19][NH:20][C:2]2[CH:11]=[CH:10][C:9]3[C:4](=[CH:5][CH:6]=[C:7]([NH:21][C:22]4[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=4)[CH:8]=3)[N:3]=2)=[CH:16][CH:15]=1

Participants

4

Reactant 3

HCID 100093-AminopyridineHCID 6075022,6-DichloroquinolineHCID 27246835-Methyl-2-furylmethylamine

Product 1

HCID 68574330HCID 68574330, compound

Procedure

The title compound, MS: m/e=331.3 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 5-methyl-2-furanmethanamine and 3-aminopyridine.

Sources & evidence

ORD record
ord-fc5a637874614607af57484072ac6b64
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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