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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602263Generated: October 30, 2026

Chloroform → HCID 67273848, compound

https://huagongshe.com/reaction/602263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67273297HCID 67273297—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 67273848HCID 6727384816.1%

Reaction Steps

(2S)-2-(2-Ethyl-1H-imidazo[4,5-c]quinolin-1-yl)propan-1-ol (0.50 g, 1.96 mmol) was suspended in 20 mL of CCl4 under an atmosphere of N2. The mixture was treated with N-bromosuccinimide (0.35 g, 1.96 mmol), heated to reflux, and irradiated with a sunlamp. After ˜20 hours the reaction was allowed to cool to ambient temperature, then it was partitioned between CH2Cl2 and saturated NaHCO3 solution. The layers were separated; the organic layer was washed sequentially with saturated NaHCO3 solution and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give a brown foam. Chromatography (AFC, SiO2, 0-15% CMA/CHCl3) gave (11S)-8,11-dimethyl-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinoline (80 mg) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906506B2
Source datasetuspto-grants-2011_03
ORD IDord-cc639989d8f54e0dae4dd4feee677f31
Source noteuspto-grants-2011_03