Diethylamine → ethyl 4-((N,N-diethylsulfamoyl)methyl)-2-ethylcyclopentanecarboxylate

A solution of (3-(ethoxycarbonyl)-4-ethylcyclopentyl)methanesulfonic acid (3.18 g, 12.03 mmol) in DCM (10 mL) and DMF (10 mL) was cooled to about 0° C. Oxalyl chloride (24.1 mL, 48.1 mmol) was added dropwise while the temperature was kept at about 0° C. After the addition was complete, the reaction mixture was warmed to ambient temperature and stirred for about 1 h. The solvent was removed under reduced pressure. The residue was dissolved in DMF (10 mL) and then added dropwise to a solution of TEA (2.51 mL, 18.03 mmol) and diethylamine (0.937 mL, 9.02 mmol) in DMF (10 mL) at about 0° C. The reaction mixture was stirred at ambient temperature for about 16 h. The solvent was removed under reduced pressure. The material was purified by silica gel (120 g) chromatography eluting with a gradient of 10-60% EtOAc in heptane to provide ethyl 4-((N,N-diethylsulfamoyl)methyl)-2-ethylcyclopentanecarboxylate (0.570 g, 30%) as a yellow oil: LC/MS (Table 1, Method b) Rt=2.60 min; MS m/z: 320 (M+H)+.

1. customwas kept at about 0° C
2. additionAfter the addition
3. customThe solvent was removed under reduced pressure
4. dissolutionThe residue was dissolved in DMF (10 mL)
5. stirringThe reaction mixture was stirred at ambient temperature for about 16 h
6. customThe solvent was removed under reduced pressure
7. customThe material was purified by silica gel (120 g) chromatography
8. washeluting with a gradient of 10-60% EtOAc in heptane

ORD-Eintrag

ord-73d81b91b0304157a45cccf4d7fb2b86

Quelldatensatz

uspto-grants-2013_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08426411B2