Hydrochloric Acid → HCID 21109109, compound

HRID 1435712Notes

Reaction equation

HRID 1435712 reaction equation
[C:1]([C:5]1[CH:14]=[C:13]2[C:8]([C:9]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([NH:23][C:24](=[O:27])[CH2:25]Br)[CH:18]=3)=[N:10][C:11]([S:15][CH3:16])=[N:12]2)=[C:7]([NH2:28])[C:6]=1[C:29]([NH2:31])=[O:30])([CH3:4])([CH3:3])[CH3:2].[NH:32]1[CH2:37][CH2:36][O:35][CH2:34][CH2:33]1.O.Cl>C(#N)C.C(Cl)Cl>[C:1]([C:5]1[CH:14]=[C:13]2[C:8]([C:9]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([NH:23][C:24](=[O:27])[CH2:25][N:32]4[CH2:37][CH2:36][O:35][CH2:34][CH2:33]4)[CH:18]=3)=[N:10][C:11]([S:15][CH3:16])=[N:12]2)=[C:7]([NH2:28])[C:6]=1[C:29]([NH2:31])=[O:30])([CH3:4])([CH3:3])[CH3:2]

Participants

7

Procedure

To a solution of tert-butyl 5-amino-2-methylthio-4-(3-(2-bromoacetamido)-phenyl)-quinazoline-6-carboxamide (example 28a, 88 mg) in acetonitrile was added morpholine (148 μl) and the mixture was stirred for 18 h. After this time CH2Cl2 (15 ml) was added and the mixture was washed with sat. aqueous NaHCO3. The organic layer was dried (MgSO4) and concentrated in vacuo. The title compound was purified by chromatography on silica gel using CH2Cl2/MeOH=1/0 to 9/1 (v/v) as eluent. The title compound was lyophilized from a mixture of acetonitrile and water containing 1.5 equiv. of HCl.

Workup

  1. washthe mixture was washed with sat. aqueous NaHCO3
  2. dry with materialThe organic layer was dried (MgSO4)
  3. concentrationconcentrated in vacuo
  4. customThe title compound was purified by chromatography on silica gel

Sources & evidence

ORD record
ord-d5321d3dba594fcf9e2c1d53be527669
Source dataset
uspto-grants-2009_11
Patent number
US07618963B2

Reaction notes

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