反应 #329323

ord-a91039c49cf4450f8f5811f75b649b6d

反应方程式

O=Cc1cc2cccc(Cl)c2nc1Cl
2,8-dichloroquinoline-3-carboxaldehyde
CC(C)(C)[S@](N)=O
(R)-2-methyl-2-propanesulfinamide
O
Water
CC(C)(C)[S@@](=O)/N=C/c1cc2cccc(Cl)c2nc1Cl
title compound
收率 97.5%
CC(C)(C)[S@@](=O)/N=C/c1cc2cccc(Cl)c2nc1Cl
(R,E)-N-[(2,8-Dichloroquinolin-3-yl)methylidene]-2-methylpropane-2-sulfinamide
收率 97.5%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGstirring
  2. 2
    workup.WAITwas continued for 17 h at r.t
  3. 3
    过滤the resulting precipitate was filtered
  4. 4
    洗涤washed with DCM
  5. 5
    干燥The organic layer was dried (Na2SO4)
  6. 6
    浓缩concentrated in vacuo

实验过程

To a solution of 2,8-dichloroquinoline-3-carboxaldehyde (43.0 g, 0.19 mol) in anhydrous THF (500 mL) was added titanium(IV) isopropoxide (114 mL, 0.38 mol) at r.t. After stirring for 15 minutes, (R)-2-methyl-2-propanesulfinamide (23.0 g, 0.19 mol) was added and stirring was continued for 17 h at r.t. Water (1 L) was added to the reaction mixture and the resulting precipitate was filtered and washed with DCM. The organic layer was dried (Na2SO4) and concentrated in vacuo to give the title compound (61 g, 97%) as a pale yellow solid. δH (CDCl3) 9.11 (1H, s), 8.83 (1H, s), 7.93 (1H, dd, J 7.54, 1.31 Hz), 7.88 (1H, dd, J 8.22, 1.31 Hz), 7.55 (1H, t, J 7.88 Hz), 1.33 (9H, s).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08653105B2uspto-grants-2014_02