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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3H-2-Benzazepin-3-one, 7-bromo-1,2,4,5-tetrahydro- → 7-Bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine hydrochloride

HRID 508573
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HRID 508573 반응식
Br[C:2]1[CH:13]=[CH:12][C:5]2[CH2:6][C:7](=O)[NH:8][CH2:9][CH2:10][C:4]=2[CH:3]=1.[Br:14]C1C=CC2CNC(=O)CCC=2C=1>O1CCCC1>[Br:14][C:12]1[CH:5]=[CH:6][C:7]2[NH:8][CH2:9][CH2:10][CH2:4][CH2:3][C:2]=2[CH:13]=1
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참가 물질

4

반응물 2

HCID 590157143H-2-Benzazepin-3-one, 7-bromo-1,2,4,5-tetrahydro-HCID 590157187-bromo-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one

생성물 1

HCID 121488297-Bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine hydrochloride

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a 1000-mL round-bottom flask was added the mixture of 7-bromo-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one and 7-bromo-1,2,4,5-tetrahydro-3H-2-benzazepin-3-one (12.6 g, 52.4 mmol) and tetrahydrofuran (260 mL). The solution was cooled to 0° C. and borane-methylsulfide complex (12.4 mL, 210 mmol) was slowly added. The reaction mixture was stirred at 0° C. for 10 min, warmed to room temperature and stirred for 3 h, then heated at reflux for 4 h. Upon cooling to room temperature, the mixture was quenched with MeOH (50 mL) to remove excess borane. The solvent was then evaporated to give 7-bromo-2,3,4,5-tetrahydro-1H-benzoazepine and 7-bromo-2,3,4,5-tetrahydro-1H-benzoazepine as sticky oil. LCMS: (FA) ES+ 226 and 228.

후처리

  1. additionTo a 1000-mL round-bottom flask was added
  2. additionborane-methylsulfide complex (12.4 mL, 210 mmol) was slowly added
  3. temperaturewarmed to room temperature
  4. stirringstirred for 3 h
  5. temperatureheated
  6. temperatureat reflux for 4 h
  7. temperatureUpon cooling to room temperature
  8. customthe mixture was quenched with MeOH (50 mL)
  9. customto remove excess borane
  10. customThe solvent was then evaporated

출처 및 근거

ORD 기록
ord-bdb4ce29037c4a868027c9525712c3a5
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096518B2

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