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Ammonia → 2-(Tetrahydro-2H-pyran-4-yl)-2-(6-(trifluoromethyl)pyridin-3-yl)ethanamine

HRID 512174
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반응식

HRID 512174 반응식
[O:1]1[CH2:6][CH2:5][C:4](=[C:7]([C:10]2[CH:11]=[N:12][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:14][CH:15]=2)[C:8]#[N:9])[CH2:3][CH2:2]1.N>CO.[Ni]>[O:1]1[CH2:2][CH2:3][CH:4]([CH:7]([C:10]2[CH:11]=[N:12][C:13]([C:16]([F:19])([F:17])[F:18])=[CH:14][CH:15]=2)[CH2:8][NH2:9])[CH2:5][CH2:6]1
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참가 물질

5

반응물 2

HCID 222AmmoniaHCID 867162002-(dihydro-2H-pyran-4(3H)-ylidene)-2-(6-(trifluoromethyl)pyridin-3-yl)acetonitrile

생성물 1

HCID 867162012-(Tetrahydro-2H-pyran-4-yl)-2-(6-(trifluoromethyl)pyridin-3-yl)ethanamine

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매2회

실험 절차

2-(Dihydro-2H-pyran-4(3H)-ylidene)-2-(6-(trifluoromethyl)pyridin-3-yl)acetonitrile (1.04 g, 3.88 mmol) was dissolved in methanol (50 mL) and 7 M NH3 in methanol (20 mL) was added. The solution was flushed with Ar. Raney nickel (0.033 g, 0.39 mmol) was added and mixture hydrogenated on a Parr Apparatus at room temperature for 4 hours. Then filtered through a plug of celite and concentrated in vacuo. The crude product was used for the next step without further purification.

후처리

  1. customThe solution was flushed with Ar
  2. filtrationThen filtered through a plug of celite and
  3. concentrationconcentrated in vacuo
  4. customThe crude product was used for the next step without further purification

출처 및 근거

ORD 기록
ord-ce784105eec3485db6208510dc41d444
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102591B2

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