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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575099Generated: October 26, 2026

3-(Trifluoromethyl)benzaldehyde → Methyl 10-bromo-9-fluoro-3-(hydroxy(3-(trifluoromethyl)phenyl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxylate

https://huagongshe.com/reaction/575099

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzaldehydeHCID 67990—
ReactantLithium ChlorideHCID 433294—
ReactantMethyl 10-bromo-9-fluoro-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxylateHCID 86693131—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 10-bromo-9-fluoro-3-(hydroxy(3-(trifluoromethyl)phenyl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxylateHCID 86693130—

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound was prepared similarly according to the procedure in Example 9. Methyl 10-bromo-9-fluoro-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxylate (150 mg, 0.44 mmol) was dissolved in THF (1.3 mL, 3 mL/mmol) and the solution was cooled to 0° C. A solution of TMPMgCl/LiCl (1 M in toluene/THF, 1.6 equiv., 0.704 mL, 0.70 mmol) was added down the side of the vial slowly. The mixture was allowed to stir for 30 minutes. After 30 minutes, 3-(trifluoromethyl)benzaldehyde (1.0 equiv., 0.06 mL, 0.44 mmol) was added and the reaction continued to stir for 30 minutes. The reaction was quenched with saturated NH4Cl and extracted 3 times with methylene chloride. The organic layers were combined, dried with Na2SO4 and concentrated. The crude was purified by flash chromatography to afford 73 mg (32.2% yield) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-a43d16bc62a94c42b9027b91430a6ab5
Source noteuspto-grants-2015_05