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2-(trifluoromethyl)-1H-indole-5-carbonitrile → (2-(Trifluoromethyl)-1h-indol-5-yl)methanamine

HRID 388381
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HRID 388381 반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[NH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([C:12]#[N:13])=[CH:7][CH:6]=2>O1CCCC1>[F:15][C:2]([F:1])([F:14])[C:3]1[NH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([CH2:12][NH2:13])=[CH:7][CH:6]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 581268122-(trifluoromethyl)-1H-indole-5-carbonitrile2회

생성물 1

HCID 58126817(2-(Trifluoromethyl)-1h-indol-5-yl)methanamine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 2-trifluoromethyl-1H-indole-5-carbonitrile (Intermediate 3, 0.16 g, 0.761 mmol) in tetrahydrofuran (5 ml) cooled in an ice-water bath, was treated with a 1M solution of borane tetrahydrofuran complex (3.05 ml, 3.05 mmol) dropwise via syringe. The reaction mixture was then left to stir under argon for 18 hrs while allowing it to warm to room temperature. The reaction mixture was then quenched with methanol (10 mL) and stirred at room temperature for 10 min. The reaction mixture was then poured onto a SCX cartridge (10 g) and washed well with methanol. The desired product was then eluted using 2M ammonia/methanol solution. Evaporation to dryness gave the title compound which was used in the next step without further purification.

후처리

  1. waitThe reaction mixture was then left
  2. customThe reaction mixture was then quenched with methanol (10 mL)
  3. stirringstirred at room temperature for 10 min
  4. additionThe reaction mixture was then poured onto a SCX cartridge (10 g)
  5. washwashed well with methanol
  6. washThe desired product was then eluted
  7. customEvaporation to dryness

출처 및 근거

ORD 기록
ord-21e994dab0cb4188859efb80266db0b0
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08377941B2

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