Reaktion #816449

Reaktionsgleichung

(4-piperazin-1-ylphenyl)amine

4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide

tert-Butyl[5-(bromomethyl)pyridin-2-yl]carbamate

potassium carbonate

→

title compound

Ausbeute 16.2%

tert-Butyl (5-{[4-[(4-morpholin-4-ylphenyl)amino]-1,1-dioxido-3-oxo-5-phenylisothiazol-2(3H)-yl]methyl}pyridin-2-yl)carbamate

Ausbeute 16.2%

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwere added
2. 2
   Einengenconcentrated
3. 3
   workup.DISSOLUTIONthe residue was dissolved in DCM
4. 4
   WaschenThe mixture was washed with water
5. 5
   Einengenconcentrated
6. 6
   Sonstigethe residue was purified

Vorschrift

(4-piperazin-1-ylphenyl)amine (0.42 g, 2.3 mmol) was added to an ice cold solution of 4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide (0.57 g, 2.3 mmol) in DMF (4 ml) and the mixture was stirred for 1 h. tert-Butyl[5-(bromomethyl)pyridin-2-yl]carbamate (0.67 g, 2.3 mmol) and anhydrous potassium carbonate (0.32 g, 2.3 mmol) were added. The reaction mixture was stirred over night, concentrated and the residue was dissolved in DCM. The mixture was washed with water and concentrated and the residue was purified using preparative HPLC to give the title compound (0.22 g, 16%). 1H NMR (400 MHz, d6-DMSO): δ 1.42 (s, 9H), 3.10-3.11 (m, 4H), 3.57-3.66 (m, 1H), 3.71-3.74 (m, 4H), 3.78-3.84 (m, 1H), 5.70 (s, 1H), 6.95-6.98 (m, 1H), 7.20-7.25 (m, 1H), 7.38-7.42 (m, 5H), 7.48-7.51 (m, 1H), 7.70-7.73 (m, 2H), 7.78 (s, 1H), 9.51 (s, 1H).

Quelle