Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773353Generated: November 1, 2026

Boron tribromide → HCID 118483141, compound

https://huagongshe.com/reaction/1773353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 118483198HCID 118483198—
SolventDichloromethaneHCID 6344—
ProductHCID 118483141HCID 11848314123%

Reaction Steps

To a solution of {1-[4-(4-cyano-3-fluoro-phenyl)-1-(3-methoxy-propyl)-6-oxo-1,6-dihydro-pyrimidin-2-yl]-piperidin-4-yl}-carbamic acid tert-butyl ester (200 mg, 0.41 mmol) in DCM was added 1M BBr3 (4 mL) at −78° C. The mixture was stirred at RT for 2 h and quenched at 0° C. with MeOH. The solution was washed with aqueous saturated NaHCO3. The organic layer was dried and concentrated. The residue was purified by preparative HPLC to give 35 mg of the title product as the hydrochloride salt (23%). 1H NMR (400 MHz, CD3OD): 1.65-1.69 (m, 2H), 1.97-2.19 (m, 4H), 3.13-3.22 (m, 2H), 3.48-3.55 (m, 1H), 3.73 (t, J=8.0 Hz, 2H), 4.55 (t, J=8.0 Hz, 2H), 4.94-4.95 (m, 2H), 6.71 (s, 1H), 7.88-8.05 (m, 3H). [M+H] Calc'd for C19H22FN5O2, 371. Found, 371.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255097B2
Source datasetuspto-grants-2016_02
ORD IDord-51e2f926a5c548458611a32402d4f72f
Source noteuspto-grants-2016_02