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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159116Generated: November 3, 2026

N-bromobutanimide → HCID 58911537, compound

https://huagongshe.com/reaction/1159116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 11176570HCID 11176570—
SolventSulfuric AcidHCID 1118—
ProductHCID 58911537HCID 5891153725.5%

Reaction Steps

A solution of (R)-8 trifluoromethyl-1,2,3,4,11,11a-hexahydro-pyrazino[1,2-b]isoquinolin-6-one (245 mg, 0.9 mmol) in H2SO4 (2 mL) was treated with NBS (210 mg, 1.17 mmol) at room temperature. After 48 h, the reaction mixture was quenched with saturated aqueous NaHCO3 and diluted with EtOAc (15 mL). The solution was extracted with EtOAc (50 mL) and the organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to afford a yellow oil. Purification of the oil by flash column chromatography (SiO2, 96:4:1 methylene chloride/methanol/triethylamine) provided (R)-10-bromo-8-trifluoromethyl-1,2,3,4,11,11a-hexahydropyrazino[1,2-b]isoquinolin-6-one (80 mg, 25%) as an off-white solid. MS (ESI) 349 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812024B2
Source datasetuspto-grants-2010_10
ORD IDord-70ff93f1b3d44dd7bfe2a7261845f8a8
Source noteuspto-grants-2010_10