Reacción #71260

Ecuación de reacción

(R)-5-bromo-2,3-dihydro-1H-inden-2-amine((1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonate

DBU

propane-2-sulfonyl chloride

→

(R)—N-(5-bromo-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide

Rendimiento 87.0%

Disolventes

DCM

DCM

HCl

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe mixture was purged with nitrogen
2. 2
   Otroto come to room temperature
3. 3
   workup.ADDITIONthe phases mixed
4. 4
   Otroseparated
5. 5
   ExtracciónThe aqueous phase was further extracted with DCM (2×100 mL)
6. 6
   Lavadobefore combined organics were washed with brine
7. 7
   ConcentraciónConcentration
8. 8
   Otrogave a light yellow oil which
9. 9
   Otrowas purified on silica eluting with 75% DCM/heptane
10. 10
    OtroDesired fractions were collected
11. 11
    Concentraciónconcentrated

Procedimiento

(R)-5-bromo-2,3-dihydro-1H-inden-2-amine((1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonate (7.88 mmol, 3.5 g) was suspended in DCM (40 mL) and DBU (23.63 mmol, 3.53 mL, 3.60 g) was added. The mixture was purged with nitrogen and cooled in an ice bath before dropwise addition of propane-2-sulfonyl chloride (15.75 mmol, 1.760 mL, 2.246 g). Stirring was continued at 0° C. for 1 h before allowing to come to room temperature. The mixture was diluted with DCM (100 mL) and 1N HCl (100 mL) and the phases mixed and separated. The aqueous phase was further extracted with DCM (2×100 mL) before combined organics were washed with brine. Concentration gave a light yellow oil which was purified on silica eluting with 75% DCM/heptane then neat DCM. Desired fractions were collected and concentrated to give (R)—N-(5-bromo-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide as a colourless oil (2.18 g, 87%). 1H NMR (400 MHz, CDCl3) δ 1.39 (d, 6H) 2.88 (m, 2H) 3.17 (sept, 1H) 3.28 (m, 2H) 4.27 (m, 2H) 7.08 (d, 1H) 7.30 (d, 1H) 7.35 (s, 1H)

Fuente