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Methyl 3-(2-amino-4-fluorophenylamino)-2-methylpropanoate → 8-fluoro-3-methyl-4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one

HRID 1485436
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HRID 1485436 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[NH:9][CH2:10][CH:11]([CH3:16])[C:12](OC)=[O:13]>C1(C)C=CC=CC=1.C([O-])(C)C.C([O-])(C)C.C([O-])(C)C.C([O-])(C)C.[Ti+4]>[F:8][C:6]1[CH:5]=[CH:4][C:3]2[NH:9][CH2:10][CH:11]([CH3:16])[C:12](=[O:13])[NH:1][C:2]=2[CH:7]=1
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참가 물질

4

반응물 1

HCID 86718504Methyl 3-(2-amino-4-fluorophenylamino)-2-methylpropanoate

생성물 1

HCID 792909248-fluoro-3-methyl-4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one수율 76%

시약·촉매·용매 2

HCID 11026Titanium isopropoxide촉매HCID 1140Toluene용매

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온도
90 °C

실험 절차

To a solution of methyl 3-(2-amino-4-fluorophenylamino)-2-methylpropanoate (10.0 g, 44.2 mmol) in toluene (200 mL) was added titanium tetraisopropanolate (18.8 g, 66.3 mmol). The mixture was stirred at 90° C. for 15 hours. The resultant mixture was concentrated in vacuo, and dissolved in tetrahydrofuran (200 mL), filtered through celite, and washed with tetrahydrofuran (100 mL). The filtrate was concentrated in vacuo, and the residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=2:1) to afford 8-fluoro-3-methyl-4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one as a black solid (6.5 g, 76%).

후처리

  1. concentrationThe resultant mixture was concentrated in vacuo
  2. dissolutiondissolved in tetrahydrofuran (200 mL)
  3. filtrationfiltered through celite
  4. washwashed with tetrahydrofuran (100 mL)
  5. concentrationThe filtrate was concentrated in vacuo
  6. customthe residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=2:1)

출처 및 근거

ORD 기록
ord-183c1f57e8fe468f894be87b18a10167
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422292B2

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