홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

TERT-BUTYL 2-CHLORONICOTINATE → HCID 22645509, 화합물

HRID 859239
노트
인쇄 미리보기

반응식

HRID 859239 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 11195236TERT-BUTYL 2-CHLORONICOTINATEHCID 57454252Monomethylamine methanol

생성물 1

HCID 22645509HCID 22645509, 화합물수율 92%

실험 절차

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).

후처리

  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)
  • 출처 및 근거

    ORD 기록
    ord-6ed74c4b7bc04db3921be1e290cbdbe8
    출처 데이터셋
    uspto-grants-2006_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07151182B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트