Diethyl Ether → 4-{[(1S,2R)-2-aminocyclohexyl]amino}-N-(2-methoxyethyl)-6-methylquinazolin-2-carboxamide

HRID 1971135노트

반응식

HRID 1971135 반응식
C(OC(=O)[NH:7][C@@H:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@@H:9]1[NH:14][C:15]1[C:24]2[C:19](=[CH:20][CH:21]=[C:22]([CH3:25])[CH:23]=2)[N:18]=[C:17]([C:26]([NH:28][CH2:29][CH2:30][O:31][CH3:32])=[O:27])[N:16]=1)(C)(C)C.C(OCC)(=O)C.Cl.C(OCC)C>C(OCC)(=O)C>[NH2:7][C@@H:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@@H:9]1[NH:14][C:15]1[C:24]2[C:19](=[CH:20][CH:21]=[C:22]([CH3:25])[CH:23]=2)[N:18]=[C:17]([C:26]([NH:28][CH2:29][CH2:30][O:31][CH3:32])=[O:27])[N:16]=1

참가 물질

5

실험 절차

To a suspension of 2.24 g of tert-butyl{(1R,2S)-2-[(2-{[(2-methoxyethyl)amino]carbonyl}-6-methylquinazolin-4-yl)amino]cyclohexyl}carbamate in 10 ml of ethyl acetate, 10 ml of a 4 N hydrogen chloride-ethyl acetate solution was added, and the mixture was stirred at room temperature for 48 hours. To the reaction solution, 20 ml of diethyl ether was added, and the mixture was stirred for 30 minutes. Then, the deposited substance was collected by filtration, washed with diethyl ether and dried under reduced pressure. The resulting powder was purified by Fuji Silysia NH silica gel column chromatography (chloroform:methanol=20:1), whereby 1.61 g of a desired compound was obtained as a colorless powder.

후처리

  1. additionwas added
  2. stirringthe mixture was stirred for 30 minutes
  3. filtrationThen, the deposited substance was collected by filtration
  4. washwashed with diethyl ether
  5. customdried under reduced pressure
  6. customThe resulting powder was purified by Fuji Silysia NH silica gel column chromatography (chloroform:methanol=20:1)

출처 및 근거

ORD 기록
ord-cac9a387d8bc4b87be7c978704ff41db
출처 데이터셋
uspto-grants-2013_04
특허 번호
US08431586B2

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