Diethylamine → HCID 86682978, compound

HRID 1497137Notes

Reaction equation

HRID 1497137 reaction equation
Cl[C:2]1[C:11]([C:12]#[N:13])=[C:10]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:20])[CH:8]=2)[N:3]=1.[CH2:21]([NH:23][CH2:24][CH3:25])[CH3:22]>>[Cl:20][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([N:23]([CH2:24][CH3:25])[CH2:21][CH3:22])[C:11]([C:12]#[N:13])=[C:10]2[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

3

Reactant 2

HCID 8021DiethylamineHCID 86682946HCID 86682946, compound

Product 1

HCID 86682978HCID 86682978, compound

Procedure

The title compound was prepared in analogy to example 27 step C from 2,6-dichloro-4-phenyl-quinoline-3-carbonitrile (prepared as described in example 27 step B) and diethylamine. Yellow solid. MS (ESI): 336.2 (M+H)+.

Sources & evidence

ORD record
ord-f50d13e28b2046e2bfd56049a82283d5
Source dataset
uspto-grants-2015_12
Patent number
US09199938B2

Reaction notes

Loading…