2-Vinylpyridine → HCID 68576809, compound

HRID 1949052Notes

Reaction equation

HRID 1949052 reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7](Cl)[CH:6]=[CH:5]2.[CH3:13][C:14]1[O:18][C:17]([CH2:19][NH2:20])=[CH:16][CH:15]=1.[CH:21]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=1)=[CH2:22]>>[CH3:13][C:14]1[O:18][C:17]([CH2:19][NH:20][C:7]2[CH:6]=[CH:5][C:4]3[C:9](=[CH:10][CH:11]=[C:2](/[CH:22]=[CH:21]/[C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=4)[CH:3]=3)[N:8]=2)=[CH:16][CH:15]=1

Participants

4

Reactant 3

HCID 75212-VinylpyridineHCID 27246835-Methyl-2-furylmethylamineHCID 128940866-Bromo-2-chloroquinoline

Product 1

HCID 68576809HCID 68576809, compound

Procedure

The title compound, MS: m/e=342.3 (M+H+), was prepared in accordance with the general method of example 2 from 6-bromo-2-chloroquinoline, 5-methyl-2-furanmethanamine and 2-vinylpyridine.

Sources & evidence

ORD record
ord-1493fdb923f042f6aa5bb264beb653a6
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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