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TERT-BUTYL 2-CHLORONICOTINATE → HCID 22645509、化合物

HRID 859239
ノート
印刷プレビュー

反応式

HRID 859239 の反応式
Cl[C:2]1[N:14]=[CH:13][CH:12]=[CH:11][C:3]=1[C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5].[CH3:15][NH2:16].CO>>[CH3:15][NH:16][C:2]1[N:14]=[CH:13][CH:12]=[CH:11][C:3]=1[C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 11195236TERT-BUTYL 2-CHLORONICOTINATEHCID 57454252Monomethylamine methanol

生成物 1

HCID 22645509HCID 22645509、化合物収率 92%

実験手順

t-Butyl 2-chloronicotinate (k) (50.0 g, 0.234 mol) was dissolved in a 40% methylamine-methanol solution (300 mL) and the mixture was stirred at room temperature for 30 h. The mixture was evaporated under reduced pressure and the resulting residue was dissolved in EtOAc (750 mL). The EtOAc solution was washed with water, dried over MgSO4 and evaporated under reduced pressure. The obtaining oily crude product was purified by a short silica gel column chromatography (ca. 300 g of silica gel, eluent: EtOAc/hexane=1/3) to give t-butyl 2-(N-methylamino)nicotinate (1) (45.0 g, ca. 92%) contaminated by starting meterial; 1H NMR (CDCl3): δ 1.57 (s, 9H), 3.05 (d, J=5.0 Hz, 3H), 6.49 (dd, J=4.6 and 7.6 Hz, 1H), 7.96 (bs, 1H), 8.04 (dd, J=2.0 and 7.6 Hz, 1H), 8.28 (dd, J=2.0 and 4.6 Hz, 1H).

後処理

  1. customThe mixture was evaporated under reduced pressure
  • dissolutionthe resulting residue was dissolved in EtOAc (750 mL)
  • washThe EtOAc solution was washed with water
  • dry with materialdried over MgSO4
  • customevaporated under reduced pressure
  • customThe obtaining oily crude product was purified by a short silica gel column chromatography (ca. 300 g of silica gel, eluent: EtOAc/hexane=1/3)
  • 出典と根拠

    ORDレコード
    ord-6ed74c4b7bc04db3921be1e290cbdbe8
    出典データセット
    uspto-grants-2006_12
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07151182B2

    反応ノート

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