Hydrochloric Acid → 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(2-(N-(t-butoxycarbonyl)-N-ethylamino)ethyloxyimino)quinazoline

HRID 220113노트

반응식

HRID 220113 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([NH:17][C:18]2[C:27]3[C:22](=[CH:23][CH:24]=[C:25](C=O)[CH:26]=3)[N:21]=[CH:20][N:19]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=1.C(OC([CH2:37][CH2:38][NH:39][CH2:40][CH2:41][O:42][NH2:43])=O)(C)(C)C.Cl.[C:45](=[O:48])(O)[O-:46].[Na+]>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([NH:17][C:18]2[C:27]3[CH2:26][C:25](=[N:43][O:42][CH2:41][CH2:40][N:39]([C:45]([O:46][C:10]([CH3:15])([CH3:11])[CH3:9])=[O:48])[CH2:38][CH3:37])[CH:24]=[CH:23][C:22]=3[N:21]=[CH:20][N:19]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=1

참가 물질

6

실험 절차

In tetrahydrofuran (1.5 ml) were dissolved 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-formylquinazoline (IV-1, 120 mg) and N-(t-butoxycarbonyl)ethylaminoethoxyamine (110 mg), and 134 μl of 2 mol/L hydrochloric acid was added, then the mixture was stirred at room temperature for 4 hours. After completion of the reaction, the reaction mixture was poured into aqueous ice-cooled saturated sodium bicarbonate solution, and extracted with ethyl acetate. The organic layer was washed with water and aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated. The resulting residue was purified by amino column chromatography (eluting with hexane:ethyl acetate=1:1), and further re-purified by silica gel chromatography (eluting with hexane:ethyl acetate=1:1) to obtain 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(2-(N-(t-butoxycarbonyl)-N-ethylamino)ethyloxyimino)quinazoline (V-16, 96 mg) as a yellow viscous oil.

후처리

  1. additionwas added
  2. customAfter completion of the reaction
  3. additionthe reaction mixture was poured into aqueous ice-
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with water and aqueous sodium chloride solution
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated
  8. customThe resulting residue was purified by amino column chromatography (eluting with hexane:ethyl acetate=1:1)
  9. customfurther re-purified by silica gel chromatography (eluting with hexane:ethyl acetate=1:1)

출처 및 근거

ORD 기록
ord-1149d957ec364d2f8f23cff88134330a
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08202879B2

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