4-Butylaniline → HCID 22417904, compound

HRID 1720278Notes

Reaction equation

[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:12][CH3:13])=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:14])[CH:3]=1.[CH2:15]([C:19]1[CH:25]=[CH:24][C:22]([NH2:23])=[CH:21][CH:20]=1)[CH2:16][CH2:17][CH3:18]>>[ClH:1].[CH2:15]([C:19]1[CH:20]=[CH:21][C:22]([NH:23][C:2]2[C:11]3[C:6](=[CH:7][C:8]([O:12][CH3:13])=[CH:9][CH:10]=3)[N:5]=[C:4]([CH3:14])[CH:3]=2)=[CH:24][CH:25]=1)[CH2:16][CH2:17][CH3:18]

Participants

Reactant 2

HCID 76944-Butylaniline

HCID 108222324-Chloro-7-methoxy-2-methylquinoline

Product 1

HCID 22417904HCID 22417904, compound

Procedure

In a manner similar to that described in Example 35, Part A, 4-chloro-7-methoxy-2-methylquinoline and 4-butylaniline were transformed into the title compound: m.p. 245°-246° C.

Sources & evidence

ORD record: ord-ef66fdd18b1b4cb5b4ac918ac90b18e2
Source dataset: uspto-grants-1996_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05506235

Reaction notes

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