Pyridine → HCID 22936754, compound

HRID 1010287Notes

Reaction equation

HRID 1010287 reaction equation
[NH2:1][C:2]1[CH:28]=[CH:27][C:5]([O:6][C:7]2[C:16]3[C:11](=[CH:12][C:13]([O:19][CH2:20][C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=4)=[C:14]([C:17]#[N:18])[CH:15]=3)[N:10]=[CH:9][CH:8]=2)=[CH:4][C:3]=1[Cl:29].[N:30]1[CH:35]=C[CH:33]=[CH:32][CH:31]=1.C1([O:42]C(Cl)=O)C=CC=CC=1.C1(N)CC1>CN(C)C=O.C(OCC)C.O>[CH2:20]([O:19][C:13]1[CH:12]=[C:11]2[C:16]([C:7]([O:6][C:5]3[CH:27]=[CH:28][C:2]([NH:1][C:35]([NH:30][CH:31]4[CH2:33][CH2:32]4)=[O:42])=[C:3]([Cl:29])[CH:4]=3)=[CH:8][CH:9]=[N:10]2)=[CH:15][C:14]=1[C:17]#[N:18])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

Participants

8

Procedure

After dissolving 4-(4-amino-3-chlorophenoxy)-7-benzyloxy-6-cyanoquinoline (8.037 g, 20.0 mmol) in dimethylformamide (40 ml) under a nitrogen atmosphere, pyridine (1.94 ml, 24.0 mmol) and phenylchloroformate (3.01 ml, 24.0 mmol) were added dropwise at room temperature and the mixture was stirred for 1 hour. Cyclopropylamine (3.46 ml, 50 mmol) was added dropwise, and the mixture was further stirred for 3 hours. Water (400 ml) and diethyl ether (400 ml) were added to the reaction solution, and after stirring overnight, the precipitated crystals were filtered out, washed with water and diethyl ether and dried at 70° C. to obtain the title compound (8.570 g, 17.7 mmol, 88.4%) as light brown crystals.

Workup

  1. stirringthe mixture was further stirred for 3 hours
  2. stirringafter stirring overnight
  3. filtrationthe precipitated crystals were filtered out
  4. washwashed with water and diethyl ether
  5. customdried at 70° C.

Sources & evidence

ORD record
ord-c5c0ba0aa62640158583f0fb75898210
Source dataset
uspto-grants-2011_07
Patent number
US07973160B2

Reaction notes

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