4-Butylaniline → HCID 22417845, compound

HRID 1720279Notes

Reaction equation

[Cl:1][C:2]1[C:11]2[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][CH:3]=1.[CH2:14]([C:18]1[CH:24]=[CH:23][C:21]([NH2:22])=[CH:20][CH:19]=1)[CH2:15][CH2:16][CH3:17]>>[OH2:12].[ClH:1].[CH2:14]([C:18]1[CH:19]=[CH:20][C:21]([NH:22][C:2]2[C:11]3[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=3)[N:5]=[CH:4][CH:3]=2)=[CH:23][CH:24]=1)[CH2:15][CH2:16][CH3:17]

Participants

Reactant 2

HCID 76944-Butylaniline

HCID 123366624-Chloro-8-methoxyquinoline

Product 1

HCID 22417845HCID 22417845, compound

Procedure

In a manner similar to that described in Example 35, Part A, 4-chloro-8-methoxyquinoline and 4-butylaniline were tranformed into the title compound: m.p. 132°-134° C.

Sources & evidence

ORD record: ord-4e9833b2c97f4469b7d12989f1551dec
Source dataset: uspto-grants-1996_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05506235

Reaction notes

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