Hexane → HCID 22466619, compound

HRID 1935038Notes

Reaction equation

HRID 1935038 reaction equation
[C:1]1(=[O:8])[O:7][C:5](=[O:6])[CH2:4][C:2]1=[CH2:3].[NH2:9][C:10]1[CH:11]=[C:12]2[C:17](=[CH:18][CH:19]=1)[N:16]=[CH:15][C:14]([C:20]#[N:21])=[C:13]2[NH:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([Br:29])[CH:24]=1.CCCCCC>C(OCC)(=O)C>[Br:29][C:25]1[CH:24]=[C:23]([NH:22][C:13]2[C:12]3[C:17](=[CH:18][CH:19]=[C:10]([NH:9][C:5](=[O:6])[CH2:4][C:2](=[CH2:3])[C:1]([OH:7])=[O:8])[CH:11]=3)[N:16]=[CH:15][C:14]=2[C:20]#[N:21])[CH:28]=[CH:27][CH:26]=1

Participants

5

Procedure

Itaconic anhydride (0.1 4 g, 1.25 mmol) was added portionwise to a solution of 0.1 g (0.30 mmol) of 6-amino-4-[(3-bromophenyl)amino]-3-quinolinecarbonitrile in 2 mL of ethyl acetate under N2. After stirring at room temperature overnight, the reaction solution was added into ice water and hexane. The product was collected, washed with water, ether and hexane, and dried in vacuo to give 0.09 g (68%) of yellowish brown solid; ESMS m/z 451.2 (M+H+).

Workup

  1. customThe product was collected
  2. washwashed with water, ether and hexane
  3. customdried in vacuo

Sources & evidence

ORD record
ord-0130b7104a224fc1894a5c0ef8ee78e3
Source dataset
uspto-grants-2002_05
Patent number
US06384051B1

Reaction notes

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