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Methanol → HCID 86625536, 화합물

HRID 2266024
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HRID 2266024 반응식
[CH3:1][O:2][N:3]([CH3:21])[C:4](=[O:20])[C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[N:7][C:6]=1[C:15]#[C:16][CH2:17][O:18][CH3:19].CO>[Pd]>[CH3:1][O:2][N:3]([CH3:21])[C:4](=[O:20])[C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[N:7][C:6]=1[CH2:15][CH2:16][CH2:17][O:18][CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 86625535HCID 86625535, 화합물

생성물 1

HCID 86625536HCID 86625536, 화합물수율 64%

시약·촉매·용매 1

HCID 23938Palladium용매

실험 절차

To a suspension of N-methoxy-2-(3-methoxy-prop-1-ynyl)-N-methyl-6-trifluoromethyl-nicotinamide (247 mg, 0.817 mmol) in 5% Pd/C (50 mg) was added CH3OH (6 ml). The mixture was purged three times with hydrogen gas (50 psi) and shaken for 2 hours at room temperature. The reaction mixture was filtered over a pad of Celite and concentrated under reduced pressure. The crude residue was chromatographed to yield the N-methoxy-2-(3-methoxy-propyl)-N-methyl-6-trifluoromethyl-nicotinamide (160 mg, 64%).

후처리

  1. customThe mixture was purged three times with hydrogen gas (50 psi)
  2. filtrationThe reaction mixture was filtered over a pad of Celite
  3. concentrationconcentrated under reduced pressure
  4. customThe crude residue was chromatographed

출처 및 근거

ORD 기록
ord-4e3e8ceeed544f6faf37e332e9e72985
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07858621B2

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