2-Vinylpyridine → HCID 68436714, compound

HRID 1170106Notes

Reaction equation

HRID 1170106 reaction equation
Br[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]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:6]2[CH:5]=[CH:4][C:3]3[C:8](=[CH:9][CH:10]=[CH:11][C:2]=3/[CH:22]=[CH:21]/[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=3)[N:7]=2)=[CH:16][CH:15]=1

Participants

4

Reactant 3

HCID 75212-VinylpyridineHCID 27246835-Methyl-2-furylmethylamineHCID 142210335-Bromo-2-chloroquinoline

Product 1

HCID 68436714HCID 68436714, compound

Procedure

The title compound, MS: m/e=342.1 (M+H+), was prepared in accordance with the general method of example 2 from 5-bromo-2-chloroquinoline, 5-methyl-2-furanmethanamine and 2-vinylpyridine.

Sources & evidence

ORD record
ord-2e3c5b5b898d45b3bb2eb84c2dd663bf
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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