Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852785Generated: October 30, 2026

N-bromobutanimide → HCID 178492795, compound

https://huagongshe.com/reaction/852785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 178440508HCID 178440508—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 178492795HCID 178492795—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5-(1-methylethyl)-2-(tricyclo[3.3.1.13,7]dec-1-ylamino)-1,3-thiazol-4(5H)-one (146 mg, 0.5 mmol) and NBS (107 mg, 0.6 mmol) in CCl4 (60 mL) was stirred at reflux for 30 min. The resulting mixture was cooled to 0° C., and filtered to remove the solid. The residue was then concentrated in vacuo and diluted with CH2Cl2 (20 mL). To this mixture was added MeOH (200 uL) and DIEA (200 uL). The mixture was stirred for 30 min, then was concentrated in vacuo and purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as white solid. MS (ES+): 323 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253196B2
Source datasetuspto-grants-2007_08
ORD IDord-2d4e45f79b8241ffbfc4e1020d225b9c
Source noteuspto-grants-2007_08