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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559703Generated: November 4, 2026

Bromotrichloromethane → HCID 59278415, compound

https://huagongshe.com/reaction/559703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrichloromethaneHCID 6383—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 59278513HCID 59278513—
SolventDichloromethaneHCID 6344—
ProductHCID 59278415HCID 59278415—

Reaction Steps

To a chilled (0° C.) solution of (R)-2-(1-{[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]-amino}-propyl)-4,5-dihydro-thiazole-4-carboxylic acid methyl ester (0.296 g, 0.670 mmol) and DBU (200 μL, 1.34 mmol) in CH2Cl2 (8.0 mL) was added BrCCl3 (69.0 μL, 0.700 mmol). The mixture was then warm to room temperature. After 18 hours, the reaction mixture was diluted with CH2Cl2 (20 mL) and washed with saturated aqueous ammonium chloride (3×10 mL). The organic layer was washed with saturated aqueous sodium bicarbonate (10 mL) and brine (10 mL), dried over MgSO4, filtered and concentrated. The mixture was purified by silica gel chromatography eluting with a gradient of 0-80% ethyl acetate in heptane to afford the title compound. MS m/z 440.77 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063065B2
Source datasetuspto-grants-2011_11
ORD IDord-3f22da6e0a3e4d35a5c58bc1bca0b596
Source noteuspto-grants-2011_11