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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182665Generated: November 2, 2026

Chlorosuccinimide → HCID 46830566, compound

https://huagongshe.com/reaction/1182665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 46830564HCID 46830564—
SolventCarbon TetrachlorideHCID 5943—
SolventDimethylformamideHCID 6228—
ProductHCID 46830566HCID 4683056645%

Reaction Conditions

Temperature0 °C

Reaction Steps

(6aR,9aS)-5,6a,7,8,9,9a-hexahydro-5-methyl-2-(4-(6-fluoropyridin-2-yl)benzyl)-cyclopent[4,5]imidazo[1,2-a]pyrrolo[4,3-e]pyrimidin-4(2H)-one (38 mg, 0.082 mmol) is dissolved in a mixture of CCl4 and DMF (8/1, v/v). The solution is cooled to 0° C., and then a solution of N-chlorosuccinimide (10.9 mg, 0.082 mmol) in CCl4 and DMF (8/1, v/v) is added dropwise. The reaction mixture is stirred at room temperature for half an hour. Solvents are removed under vacuum, and the residue is purified by a semi-preparative HPLC to give pure product as off white solids (16.5 mg, yield 45%). MS (ESI) m/z 450.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664207B2
Source datasetuspto-grants-2014_03
ORD IDord-a19285ed96974da2939911290f36a9f0
Source noteuspto-grants-2014_03