Triethylamine → 2,2,2-trifluoro-N-[4-(1-piperidinesulfonylpiperidin-4-ylmethyl)-phenyl]acetamide

Temperature

2.5 °C

A solution of 2,2,2-trifluoro-N-(4-(piperidin-4-ylmethyl)-phenyl]acetamide (0.5 g, 1.75 mmol) (prepared as previously described in Example 19, steps 1 to 3) and triethylamine in dichloromethane (10 mL) was cooled in an ice bath under a nitrogen atmosphere. The mixture was then treated with a solution of 1-piperidinesulfonyl chloride (0.39 g, 2.09 mmol) in dichloromethane (1 mL). The reaction mixture was stirred for 1.5 hours at 0-5° C. and quenched with water. The organic layer was separated, and the aqueous layer extracted with dichloromethane. The combined organic extracts were washed with water and brine, dried, and solvents removed in vacuo. The residue was chromatographed on silica gel, eluting with 30% ethyl acetate/hexanes, to give 2,2,2-trifluoro-N-[4-(1-piperidinesulfonylpiperidin-4-ylmethyl)-phenyl]acetamide (0.48 g) as a white solid, m.p. 156-157° C.; Analysis for C19H26N3O3SF3: Calc.: C, 52.64; H, 6.05; N, 9.69; Found: C, 52.84; H, 6.00; N, 6.79.

1. temperaturewas cooled in an ice bath under a nitrogen atmosphere
2. customquenched with water
3. customThe organic layer was separated
4. extractionthe aqueous layer extracted with dichloromethane
5. washThe combined organic extracts were washed with water and brine
6. customdried
7. customsolvents removed in vacuo
8. customThe residue was chromatographed on silica gel
9. washeluting with 30% ethyl acetate/hexanes

ORD record

ord-07988dad74c948f9b3630d5091e63cda

Source dataset

uspto-grants-2001_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06184242B2