反応 #2286396

ord-add0240209f04be6a1c43e7523a06f1d

反応方程式

CCNC(=S)N(C)c1sc(-c2cccnc2)nc1C
3-ethyl-1-methyl-1-(4-methyl-2-(pyridin-3-yl)thiazol-5-yl)thiourea
CCI
iodoethane
CCN=C(SCC)N(C)c1sc(-c2cccnc2)nc1C
title compound
収率 39.2%
CCN=C(SCC)N(C)c1sc(-c2cccnc2)nc1C
2,3-diethyl-1-methyl-1-(4-methyl-2-pyridin-3-yl-thiazol-5-yl)-isothiourea
収率 39.2%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度Upon cooling the solvent
  2. 2
    その他was removed under reduced pressure
  3. 3
    その他the residue purified via silica gel chromatography (0 to 100% ethyl acetate/hexanes)

実験手順

A solution of 3-ethyl-1-methyl-1-(4-methyl-2-(pyridin-3-yl)thiazol-5-yl)thiourea (70 mg, 0.239 mmol) and iodoethane (74.7 mg, 0.479 mmol) in ethanol (5 mL) was heated at 80° C. for 6 h in a sealed tube. Upon cooling the solvent was removed under reduced pressure and the residue purified via silica gel chromatography (0 to 100% ethyl acetate/hexanes) to furnish the title compound as a clear oil (30 mg, 39%): 1H NMR (400 MHz, CDCl3) δ 9.10 (d, J=2.0 Hz, 1H), 8.64 (dd, J=4.6 Hz, 1.4 Hz, 1H), 8.20 (d, J=4.2 Hz, 1H), 7.41-7.37 (m, 1H), 3.63 (q, J=7.6 Hz, 2H), 3.22 (s, 3H), 2.72 (q, J=7.8 Hz, 2H), 2.38 (s, 3H), 1.28-1.17 (m, 6H); ESIMS m/z 321 (M+1).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09357780B2uspto-grants-2016_06