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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178982Generated: October 31, 2026

Hydrochloric Acid → HCID 11247975, compound

https://huagongshe.com/reaction/1178982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
Reactant2-Chloro-4,6-dimethoxy-1,3,5-triazineHCID 18450—
Reactant4-AminotetrahydropyranHCID 419223—
ReactantHCID 58975136HCID 58975136—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11247975HCID 11247975—

Reaction Conditions

Temperature5 °C

Reaction Steps

Stir a solution of 4-(3-cyclopentyl-indole-1-sulfonyl)-benzoic acid (19.0 g, 51.43 mmol) in anhydrous THF (250 mL), cool to 5° C., add N-methylmorpholine (5.8 mL, 52.72 mmol) and 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) (9.0 g, 51.34 mmol). Stir the mixture at 0-5° C. for 1 h, add a solution of 4-aminotetrahydro-pyran (5.8 g, 57.36 mmol) in dry THF (75 mL) via dropping funnel. Bring the mixture to room temperature, stir for 3 h, and cool back down to 5° C. Stir the mixture and add 1N HCl (250 mL), add the resulting solution to a separatory funnel, and extract with ethyl acetate (250 mL). Separate the layers, wash the organic layer with brine (250 mL), and combine the aqueous layers and extract with ethyl acetate (250 mL). Combine the organics and wash with saturated aqueous sodium bicarbonate (400 mL) and dry the organic layer over sodium sulfate. Concentrate to give a foam, dissolve in minimum methylene chloride, and add to a biotage flash 65M cartridge. Elute with 3:2 hexanes/ethyl acetate to provide the major product as a foam, and dry (20 mm Hg, 40° C.) to give a white powder of pure product (20.3 g, 87%); MS (ESI) m/z 453 (m+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276516B2
Source datasetuspto-grants-2007_10
ORD IDord-3afe47aa07394d42baf708b8e6e132e3
Source noteuspto-grants-2007_10