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Chlorotrimethylsilane → Methyl 6-(cyclohexylamino)-5-nitronicotinate

HRID 392980
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HRID 392980 반응식
[CH:1]1([NH:7][C:8]2[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[CH:10][N:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[Si](C)(C)[CH3:22]>CO>[CH:1]1([NH:7][C:8]2[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][C:11]([C:12]([O:14][CH3:22])=[O:13])=[CH:10][N:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 6397Chlorotrimethylsilane2회HCID 226607816-(Cyclohexylamino)-5-nitronicotinic acid

생성물 1

HCID 22660792Methyl 6-(cyclohexylamino)-5-nitronicotinate수율 89%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of intermediate 57 (9.7 g, 32.2 mmol) in methanol (400 mL) was added chlorotrimethylsilane (3 mL) to achieve pH=2. The reaction mixture was heated at strong reflux for 72 h, during which time the pH was monitored and more chlorotrimethylsilane added as necessary to maintain an acidic solution. The reaction mixture was allowed to cool and was then concentrated on a rotary evaporator. The residue was purified by column chromatography (silica gel, 7:2:1 hexanes/dichloromethane/methanol) to afford the crude ester as a yellow solid (9.0 g, 89%). ESI-MS m/e 280.1 (M+1).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat strong reflux for 72 h, during which time the pH
  3. temperatureto maintain an acidic solution
  4. temperatureto cool
  5. concentrationwas then concentrated on a rotary evaporator
  6. customThe residue was purified by column chromatography (silica gel, 7:2:1 hexanes/dichloromethane/methanol)

출처 및 근거

ORD 기록
ord-437bcbb96a0d44e6b31e4f90f94328c5
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06803374B2

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