Toluene → 4-(4-Chloro-2-fluoroanilino)-6-methoxy-7-(2-(methylamino)ethoxy)quinazoline hydrochloride hydrate

HRID 1384603노트

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HRID 1384603 반응식
C(O)(C(F)(F)F)=[O:2].[Cl:8][C:9]1[CH:39]=[CH:38][C:12]([NH:13][C:14]2[C:23]3[C:18](=[CH:19][C:20]([O:26][CH2:27][CH2:28][N:29](C)[C:30](OC(C)(C)C)=O)=[C:21]([O:24][CH3:25])[CH:22]=3)[N:17]=[CH:16][N:15]=2)=[C:11]([F:40])[CH:10]=1.C1(C)C=CC=CC=1>C(Cl)Cl>[OH2:2].[ClH:8].[Cl:8][C:9]1[CH:39]=[CH:38][C:12]([NH:13][C:14]2[C:23]3[C:18](=[CH:19][C:20]([O:26][CH2:27][CH2:28][NH:29][CH3:30])=[C:21]([O:24][CH3:25])[CH:22]=3)[N:17]=[CH:16][N:15]=2)=[C:11]([F:40])[CH:10]=1

참가 물질

5

실험 절차

TFA (4 ml) was added to a solution of 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(N-methyl-N-t-butoxycarbonylamino)ethoxy)quinazoline (390 mg, 0.82 mmol) in methylene chloride (4 ml) and the mixture stirred for 2 hours at ambient temperature. Toluene was added and the volatiles were removed by evaporation. The residue was dissolved in methylene chloride and 3M ethereal hydrogen chloride (1 ml) was added. The resulting precipitate was collected by filtration, washed with ether and dried under vacuum to give 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(methylamino)ethoxy)quinazoline hydrochloride hydrate (290 mg; 79%). 1H NMR Spectrum: (DMSOd6; CF3COOD) 2.74(s, 3H); 3.53(t, 2H); 4.05(s, 3H); 4.53(t, 2H); 7.46(d, 1H); 7.47(s, 1H); 7.6-7.7(m, 2H); 8.24(s, 1H); 8.91(s, 1H) MS-ESI: 377 [MH]+

후처리

  1. customthe volatiles were removed by evaporation
  2. dissolutionThe residue was dissolved in methylene chloride
  3. addition3M ethereal hydrogen chloride (1 ml) was added
  4. filtrationThe resulting precipitate was collected by filtration
  5. washwashed with ether
  6. customdried under vacuum

출처 및 근거

ORD 기록
ord-e4c7fef4f2b6422495bc38e765d21b5d
출처 데이터셋
uspto-grants-2001_07
특허 번호
US06258951B1

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