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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594911Generated: October 31, 2026

Water → HCID 86724315, compound

https://huagongshe.com/reaction/594911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantN-methylhydroxylamine hydrochlorideHCID 77906—
ReactantHCID 86724316HCID 86724316—
SolventEthanolHCID 702—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 86724315HCID 8672431560.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of N-[5″,5″-difluoro-6′-(pyrimidin-5-yl)-5″,6″-dihydrodispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]thiazin]-2″-yl]benzamide (76 mg, 0.16 mmol) in ethanol (4 mL) were added N-hydroxymethanamine hydrochloride (133 mg, 1.59 mmol) and pyridine (126 mg, 1.59 mmol), and the mixture was stirred for 27 hours at 70° C. After cooling, H2O and brine were added and the mixture was extracted with chloroform. The organic layer was dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography (EtOAc/hexane=50:50-100:0 and then EtOH/CHCl3=5:95) and a resultant solid was washed with iPr2O to give 5″,5″-difluoro-6′-(pyrimidin-5-yl)-5″,6″-dihydrodispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]thiazin]-2″-amine (36 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242973B2
Source datasetuspto-grants-2016_01
ORD IDord-1532135ca9f940de9170f9847829718f
Source noteuspto-grants-2016_01