Allylamine → HCID 44217829, compound

HRID 1669703Notes

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

Participants

Reactant 3

HCID 7853Allylamine

HCID 27246835-Methyl-2-furylmethylamine

HCID 142210335-Bromo-2-chloroquinoline

Product 1

HCID 44217829HCID 44217829, compound

Procedure

The title compound, MS: m/e=294.4 (M+H+), was prepared in accordance with the general method of example 3 from 5-bromo-2-chloroquinoline, 5-methyl-2-furanmethanamine and allylamine.

Sources & evidence

ORD record: ord-f1dcb398577b4f439651d6e7d3b41b7e
Source dataset: uspto-grants-2011_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07989628B2

Reaction notes

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