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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888004Generated: November 2, 2026

Hydrochloric Acid → HCID 86655246, compound

https://huagongshe.com/reaction/1888004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantHCID 86655248HCID 86655248—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86655246HCID 86655246—

Reaction Steps

Deprotection/protection: To a solution of N-(1-{4-[(6-chloro-3-nitropyridin-2-yl)amino]phenyl}-1-methylethyl)-2-methylpropane-2-sulfinamide (107 mg) in DCM (5 ml) was added dropwise a solution of hydrogen chloride in dioxane (4 M, 130 ul) at room temperature. The reaction mixture was stirred for 30 min. Hexane was added to the suspension and the solid was filtered to give N-[4-(1-amino-1-methylethyl)phenyl]-6-chloro-3-nitropyridin-2-amine hydrochloride. To a suspension of N-[4-(1-amino-1-methylethyl)phenyl]-6-chloro-3-nitropyridin-2-amine hydrochloride in THF (3 ml) chilled to 0° C. was added saturated sodium bicarbonate solution (6 ml) and followed by a solution of di-tert-butyl dicarbonate (167 mg) in THF (3 ml) dropwise. After being stirred at room temperature over night, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate solution and brine. The organics were dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by column chromatography (3-30% ethyl acetate in hexanes) gave the product (99 mg, 2 steps 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501770B2
Source datasetuspto-grants-2013_08
ORD IDord-7f53fd50145942c4bd08d563867e47fc
Source noteuspto-grants-2013_08