Lawesson's reagent → (4-Isopropyl-piperazin-1-yl)-(5-piperidin-1-ylmethyl-furan-2-yl)-methanethione

HRID 33749

반응식

HRID 33749 반응식
[CH:1]([N:4]1[CH2:9][CH2:8][N:7]([C:10]([C:12]2[O:13][C:14]([CH2:17][N:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[CH:15][CH:16]=2)=O)[CH2:6][CH2:5]1)([CH3:3])[CH3:2].COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:33])=CC=1>C1COCC1>[CH:1]([N:4]1[CH2:9][CH2:8][N:7]([C:10]([C:12]2[O:13][C:14]([CH2:17][N:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[CH:15][CH:16]=2)=[S:33])[CH2:6][CH2:5]1)([CH3:3])[CH3:2]

참가 물질

4

반응 조건

온도
70 °C

실험 절차

A solution of (4-isopropyl-piperazin-1-yl)-(5-piperidin-1-ylmethyl-furan-2-yl)-methanone (Example 1, 1 equiv.) and Lawesson's reagent (2.1 equiv.) in THF is heated at reflux (70° C.) for 48 h. The reaction is cooled to room temperature and the solvent is removed in vacuo. Chromatography of the residue on a silica gel column using 1-6% 2 M NH3 in MeOH/DCM) provides the title compound.

후처리

  1. temperatureThe reaction is cooled to room temperature
  2. customthe solvent is removed in vacuo

출처 및 근거

ORD 기록
ord-1110e46f7d2f433e8f777fa8a0a330e1
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07429659B2

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