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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927891Generated: November 3, 2026

HCID 86324392, compound → HCID 71006847, compound

https://huagongshe.com/reaction/927891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86324392HCID 86324392—
Reactant(1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acidHCID 86713249—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
ProductHCID 71006847HCID 7100684746.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of (1aRS,7bSR)-5-(2-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylic acid (Intermediate 67, 0.2 g) and 2-((R)-1-ethylpyrrolidin-3-yl)ethylamine (Intermediate 203, 2.0 g) in DMSO (2 mL) was divided between two sealed vials and each was stirred and heated at 130° C. for 24 hours. After cooling, the combined mixture was diluted with methanol and then concentrated under vacuum. The residue was purified by HPLC (C18) to give (1aRS,7bSR)-5-{2-[2-((R)-1-ethylpyrrolidin-3-yl)ethylamino]-benzenesulfonyl-amino}-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid (0.125 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-8f10a5eafd6b468c807b118a8e3d1c3b
Source noteuspto-grants-2016_03