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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189040Generated: October 31, 2026

N-bromobutanimide → HCID 86653752, compound

https://huagongshe.com/reaction/2189040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 86653751HCID 86653751—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 86653752HCID 86653752—

Reaction Conditions

Temperature60 °C

Reaction Steps

Suspend 100 mg (0.236 mmol) of (+/−)-cis-({3-[(5-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]cyclohexyl}oxy)acetic acid tert-butyl ester in 0.2 ml of tetrachloromethane and add 46.1 mg (0.259 mmol) of NBS. Stir the reaction mixture at 60° C. for a total of 2 h, and add a further 23 mg of NBS after 1 h. After cooling, remove the tetrachloromethane under reduced pressure and purify the residue by preparative RP-HPLC (eluent: acetonitrile/water). 43.6 mg (36.8% of theory) of the target product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324222B2
Source datasetuspto-grants-2012_12
ORD IDord-356d5950a43c4e6ea14fa789c2f1c291
Source noteuspto-grants-2012_12