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Triphenylphosphine → 4-(4-Chloro-2-fluoroanilino)6-methoxy-7-(2-(3-oxomorpholino)ethoxy)quinazoline hydrochloride

HRID 1838585
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HRID 1838585 반응식
N(C(OCC)=O)=NC(OCC)=O.[Cl:13][C:14]1[CH:33]=[CH:32][C:17]([NH:18][C:19]2[C:28]3[C:23](=[CH:24][C:25]([OH:31])=[C:26]([O:29][CH3:30])[CH:27]=3)[N:22]=[CH:21][N:20]=2)=[C:16]([F:34])[CH:15]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O[CH2:55][CH2:56][N:57]1[CH2:62][CH2:61][O:60][CH2:59][C:58]1=[O:63]>C(Cl)Cl.C1COCC1>[ClH:13].[Cl:13][C:14]1[CH:33]=[CH:32][C:17]([NH:18][C:19]2[C:28]3[C:23](=[CH:24][C:25]([O:31][CH2:55][CH2:56][N:57]4[CH2:62][CH2:61][O:60][CH2:59][C:58]4=[O:63])=[C:26]([O:29][CH3:30])[CH:27]=3)[N:22]=[CH:21][N:20]=2)=[C:16]([F:34])[CH:15]=1
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참가 물질

7

반응물 4

HCID 11776Triphenylphosphine2회HCID 220568ethyl N-ethoxycarbonyliminocarbamate2회HCID 152874004-(2-Hydroxyethyl)morpholin-3-one2회HCID 1355137204-(4-Chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazoline

생성물 1

HCID 187534774-(4-Chloro-2-fluoroanilino)6-methoxy-7-(2-(3-oxomorpholino)ethoxy)quinazoline hydrochloride
수율 79.6%

시약·촉매·용매 2

HCID 6344Dichloromethane용매2회HCID 8028Tetrahydrofuran용매

실험 절차

Diethyl azodicarboxylate (400 mg, 2.3 mmol) was added dropwise to a mixture of 4-(4-chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (250 mg, 0.78 mmol), (prepared as described for the starting material in Example 2), triphenylphosphine (615 mg, 2.3 mmol) and 4-(2-hydroxyethyl)-3-morpholinone (170 mg, 1.17 mmol), (EP 580402A2), in methylene chloride (5 ml) under nitrogen. The mixture was stirred for 4 hours at ambient temperature, methylene chloride (5 ml) was added and stirring was continued for a further 18 hours at ambient temperature. THF (5 ml), 4-(2-hydroxyethyl)-3-morpholinone (113 mg, 0.78 mmol), triphenylphosphine (204 mg, 0.78 mmol) were added and diethyl azodicarboxylate (136 mg, 0.78 mmol) was then added dropwise. The mixture was stirred for 5 minutes at ambient temperature, and was purified by pouring directly onto a silica column, eluting with methylene chloride/ethyl acetate/methanol (5/4/1). The purified solid was dissolved in methylene chloride and 2M methanolic hydrogen chloride (0.5 ml) was added. The mixture was concentrated by evaporation and then diluted with ether. 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-(3-oxomorpholino)ethoxy)quinazoline hydrochloride (150 mg, 39%).

후처리

  1. custom(prepared
  2. stirringstirring
  3. waitwas continued for a further 18 hours at ambient temperature
  4. stirringThe mixture was stirred for 5 minutes at ambient temperature
  5. customwas purified
  6. additionby pouring directly onto a silica column
  7. washeluting with methylene chloride/ethyl acetate/methanol (5/4/1)
  8. dissolutionThe purified solid was dissolved in methylene chloride
  9. addition2M methanolic hydrogen chloride (0.5 ml) was added
  10. concentrationThe mixture was concentrated by evaporation
  11. additiondiluted with ether
  12. filtrationThe resulting precipitate was collected by filtration
  13. washwashed with ether
  14. customdried under vacuum

출처 및 근거

ORD 기록
ord-d2adb8acf2fe442ebc6f7aef9c5629d4
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06673803B2

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