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Lithium hexamethyldisilazane → 4-Chloro-6-methoxynicotinimidamide hydrochloride

HRID 886105
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HRID 886105 반응식
[Cl:1][C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[C:4]([O:10][CH3:11])[CH:3]=1.[Li+].C[Si]([N-:17][Si](C)(C)C)(C)C>C1COCC1>[ClH:1].[Cl:1][C:2]1[C:7]([C:8]([NH2:17])=[NH:9])=[CH:6][N:5]=[C:4]([O:10][CH3:11])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2733832Lithium hexamethyldisilazaneHCID 582043184-Chloro-6-methoxypyridine-3-carbonitrile

생성물 1

HCID 670506614-Chloro-6-methoxynicotinimidamide hydrochloride

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 4-chloro-6-methoxy-nicotinonitrile (10.1 g, 59.7 mmol) in THF (300 mL) at −78° C. was added LiHMDS (65.7 mL) dropwise and the reaction mixture stirred for 30 min before allowing to warm to RT and stirring for a further 1 h. The reaction was quenched by the addition of 1N HCl (to pH˜1) and then extracted three times with ethyl acetate. The aqueous layer was concentrated in vacuo to give brown solid which was azeotroped with toluene to give the title compound as a tan solid. Mixture with ammonium chloride, 72% title compound by weight. (15.2 g, 83%). 1H NMR 400 MHz (DMSO-d) δ: 9.68 (4H, d, J=15.79 Hz), 8.46 (1H, s), 7.47 (5H, t, J=50.66 Hz), 7.27 (1H, s), 3.95 (3H, s).

후처리

  1. stirringstirring for a further 1 h
  2. customThe reaction was quenched by the addition of 1N HCl (to pH˜1)
  3. extractionextracted three times with ethyl acetate
  4. concentrationThe aqueous layer was concentrated in vacuo
  5. customto give brown solid which
  6. customwas azeotroped with toluene

출처 및 근거

ORD 기록
ord-81404e9acecc4034b0fa7a958abe01db
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242104B2

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