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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928040Generated: October 31, 2026

Methyl 5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate → HCID 77979772, compound

https://huagongshe.com/reaction/928040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-amino-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylateHCID 86713293—
ReactantHCID 86713352HCID 86713352—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 77979772HCID 7797977260.3%

Reaction Steps

A solution of 2-(4-ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzenesulfonyl chloride (Intermediate 174, 0.368 g) and methyl (1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate (Intermediate 42, 0.219 g) in pyridine (3 mL) and DCM (3 mL) was left to stand at room temperature for 17 hours. The mixture was evaporated in vacuo and the residue was dissolved in water and DCM and the organic layer was dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 50-100% to give a gum which was triturated with ether and filtered to give methyl (1aRS,7bSR)-5-[2-(4-ethyl-2-oxopiperazin-1-ylmethyl)-4-fluorobenzenesulfonylamino]-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-4-carboxylate (0.312 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-915672c7be9d4032875364f2175d62f2
Source noteuspto-grants-2016_03