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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928027Generated: October 30, 2026

2-Bromobenzenesulfonyl chloride → HCID 71006886, compound

https://huagongshe.com/reaction/928027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzenesulfonyl chlorideHCID 520403—
ReactantMethyl 5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylateHCID 86713293—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 71006886HCID 7100688676.5%

Reaction Steps

2-Bromobenzenesulfonyl chloride (0.559 g) was added to a solution of methyl (1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate (Intermediate 42, 0.40 g) in DCM (12 mL) and pyridine (4 mL) and the resultant mixture was stirred at room temperature for 1 hour. The mixture was evaporated to dryness and the residue was dissolved in DCM and washed with 2N HCl, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-35% to give methyl (1aRS,7bSR)-5-(2-bromo-benzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate (0.612 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-c74d68c0a722497e9b476bec5bbbedbf
Source noteuspto-grants-2016_03