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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423361Generated: November 3, 2026

Allyl bromide → HCID 178456206, compound

https://huagongshe.com/reaction/1423361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
ReactantHCID 178430818HCID 178430818—
SolventTetrahydrofuranHCID 8028—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178456206HCID 17845620654.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 1-methyl-3H-pyrrolo[2,3-c]quinolin-4-ol (1.2 g, 6.05 mmol) in a mixture of THF (30 mL) and NMP (60 mL) was treated with Cs2CO3 (2.95 g, 9.08 mmol). Allyl bromide (0.524 mL, 6.06 mmol) was added dropwise, and the resulting mixture was stirred at 40° C. for 12 h. The mixture was cooled and quenched with aqueous HCl (1 N) and EtOAc. The organic layer was separated, washed with aqueous HCl (1 N), brine, and dried over Na2SO4. Filtration and removal of the volatiles gave a residue that was triturated with Et2O to give the title compound (0.78 g, 54%) as a solid. LCMS (ES+) m/z 239 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927569B2
Source datasetuspto-grants-2015_01
ORD IDord-c405bfabf2424e459828da0a6946a40e
Source noteuspto-grants-2015_01