Diethyl Ether → HCID 178496012, compound

HRID 75527Notes

Reaction equation

HRID 75527 reaction equation
[C:1]([NH:4][C@@H:5]1[CH2:10][CH2:9][CH2:8][CH2:7][C@@H:6]1[NH:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[C:19]([CH3:22])[CH:20]=2)[N:15]=[C:14]([C:23]([NH:25][CH2:26][CH2:27][O:28][CH3:29])=[O:24])[N:13]=1)(=[NH:3])[CH3:2].C(OCC)(=O)C.[ClH:36].C(OCC)C>C(OCC)(=O)C>[ClH:36].[ClH:36].[C:1]([NH:4][C@@H:5]1[CH2:10][CH2:9][CH2:8][CH2:7][C@@H:6]1[NH:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[C:19]([CH3:22])[CH:20]=2)[N:15]=[C:14]([C:23]([NH:25][CH2:26][CH2:27][O:28][CH3:29])=[O:24])[N:13]=1)(=[NH:3])[CH3:2]

Participants

5

Procedure

To a solution of 391 mg of 4-{[(1S,2R)-2-(ethanimidoylamino)cyclohexyl]amino}-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide in 5 ml of ethyl acetate, 3 ml of a 4 N hydrogen chloride-ethyl acetate solution was added, and the mixture was stirred for 10 minutes. Then, to the reaction solution, 10 ml of diethyl ether was added, and the deposited substance was collected by filtration, washed with diethyl ether and dried under reduced pressure, whereby 405 mg of a desired compound was obtained as a white powder.

Workup

  1. filtrationthe deposited substance was collected by filtration
  2. washwashed with diethyl ether
  3. customdried under reduced pressure

Sources & evidence

ORD record
ord-abda336c8f7a40fbab07ab27570a8fec
Source dataset
uspto-grants-2014_09
Patent number
US08835446B2

Reaction notes

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