반응 #67121

반응 방정식

6-Bromo-4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-1-(phenylsulfonyl)-1H-indazole

6-oxa-9-azaspiro[4.5]decane

DIPEA

sodium iodide

→

title compound

수율 30.0%

9-({5-[6-Bromo-1-(phenylsulfonyl)-1H-indazol-4-yl]-1,3,4-oxadiazol-2-yl}methyl)-6-oxa-9-azaspiro[4.5]decane

수율 30.0%

용매

DCM

acetonitrile

반응 조건

후처리

1. 1
   온도cooled
2. 2
   세척washed with aqueous HCl
3. 3
   기타The organic layer was separated
4. 4
   세척washed with water
5. 5
   기타the solvent removed under a stream of nitrogen
6. 6
   기타The resulting residue was purified
7. 7
   세척eluting with 0-100% ethyl acetate/cyclohexane over 40 mins
8. 8
   기타evaporated

실험 절차

6-Bromo-4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-1-(phenylsulfonyl)-1H-indazole (200 mg, 0.441 mmol) in acetonitrile (2 ml) was treated with 6-oxa-9-azaspiro[4.5]decane (160 mg, 0.793 mmol), DIPEA (0.154 ml, 0.8825 mmol) and sodium iodide (66 mg, 0.44 mmol). The reaction mixture was heated at 70° C. for 5 h, then cooled, diluted with DCM and washed with aqueous HCl. The organic layer was separated using a hydrophobic frit, washed with water and the solvent removed under a stream of nitrogen. The resulting residue was purified by loading onto a silica cartridge (20 g) and eluting with 0-100% ethyl acetate/cyclohexane over 40 mins. The appropriate fractions were combined and evaporated to give the title compound as a yellow solid (74 mg).

출처