Hydrochloric Acid → HCID 67998124, compound

To a solution of N-((1S,3S,4R)-3-(3-allyl-6-tosyl-6H-imidazo[1,5-a]pyrrolo[2,3-e]pyrazin-1-yl)-4-ethylcyclopentyl)cyclopropanesulfonamide (0.28 g, 0.48 mmol, prepared using H with Preparation #12, Preparation #Z.1, HATU and DIEA, Q with Lawesson's reagent and mercury (II) trifluoroacetate) in 1,4-dioxane (5 mL) and water (1.5 mL) was added sodium periodate (0.21 g, 0.97 mmol) followed by osmium tetroxide (4 wt % in water, 0.19 mL, 0.024 mmol). After about 4 h, the reaction mixture was diluted with DCM (10 mL) and water (10 mL), the organic layer was separated and concd in vacuo. The crude aldehyde was dissolved in EtOH (5 mL) and NaBH4 (0.18 g, 4.8 mmol) was added to the reaction mixture. After about 4 h, HCl (1 N aqueous, 10 mL) and DCM (20 mL) were added to the reaction mixture. The organic layer was separated and concd in vacuo. The residue was purified by silica gel chromatography eluting with EtOAc in DCM to give crude alcohol (0.061 g). To a solution of the crude alcohol in DCM (1 mL) was added DIEA (0.047 mL, 0.27 mmol) followed by methanesulfonyl chloride (0.0092 mL, 0.12 mmol). After about 2 h, the reaction mixture was diluted with DCM (10 mL) and saturated aqueous NaHCO3 (10 mL). The organic layer was separated, concd in vacuo, and diluted with DMF (1.0 mL). Sodium methanethiolate (0.075 g, 1.1 mmol) was added to the reaction mixture. After stirring at ambient temperature for about 15 h, the reaction mixture was heated to about 50° C. After about 4 h, the reaction mixture was cooled to ambient temperature and diluted with DCM (10 mL) and saturated aqueous NaHCO3 (10 mL). The organic layer was separated, concd in vacuo, and purified by chromatography on silica gel (40 g) eluting with 20-80% MeCN in DCM. The fractions containing the thioether were combined and concd in vacuo. The crude thioether was dissolved in DCM (1 mL) and treated with OXONE® tetrabutylammonium salt (0.114 g, 0.320 mmol). After about 4 h, the reaction mixture was diluted with DMSO (1 mL) and partially concd in vacuo to remove DCM. The crude mixture was purified by RP-HPLC (Table 1, Method k). The fractions containing the desired sulfone were combined and concd in vacuo. The residue was further purified by chromatography on silica gel (12 g) eluting with 5% MeOH in DCM to provide N-((1S,3R,4S)-3-ethyl-4-(3-(2-(methylsulfonyl)ethyl)-6H-imidazo[1,5-a]pyrrolo[2,3-e]pyrazin-1-yl)cyclopentyl)cyclopropanesulfonamide (0.002 g, 1.4%) as a solid: LC/MS (Table 1, Method a) Rt=1.82 min; MS m/z: 480 (M+H)+.

1. customthe organic layer was separated
2. dissolutionThe crude aldehyde was dissolved in EtOH (5 mL)
3. waitAfter about 4 h
4. customThe organic layer was separated
5. customThe residue was purified by silica gel chromatography
6. washeluting with EtOAc in DCM
7. customto give crude alcohol (0.061 g)
8. waitAfter about 2 h
9. customThe organic layer was separated
10. additionconcd in vacuo, and diluted with DMF (1.0 mL)
11. temperaturethe reaction mixture was heated to about 50° C
12. waitAfter about 4 h
13. temperaturethe reaction mixture was cooled to ambient temperature
14. customThe organic layer was separated
15. customconcd in vacuo, and purified by chromatography on silica gel (40 g)
16. washeluting with 20-80% MeCN in DCM
17. additionThe fractions containing the thioether
18. dissolutionThe crude thioether was dissolved in DCM (1 mL)
19. waitAfter about 4 h
20. customto remove DCM
21. customThe crude mixture was purified by RP-HPLC (Table 1, Method k)
22. additionThe fractions containing the desired sulfone
23. customThe residue was further purified by chromatography on silica gel (12 g)
24. washeluting with 5% MeOH in DCM

ORD record

ord-9a8eaead65b74a9cbffb3d19a742d202

Source dataset

uspto-grants-2013_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08426411B2