HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559699Generated: October 30, 2026
Bromotrichloromethane → HCID 59278232, compound
https://huagongshe.com/reaction/559699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromotrichloromethane | HCID 6383 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 66727508 | HCID 66727508 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59278232 | HCID 59278232 | — |
Reaction Steps
To a chilled (0° C.) solution of (4S,5S)-2-(1-{[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]-amino}-propyl)-5-methyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester (0.529 g, 1.20 mmol) and DBU (360 μL, 2.40 mmol) in CH2Cl2 (10.0 mL) was added BrCCl3 (125 μL, 1.26 mmol). The mixture was then warmed to room temperature. After 18 hours, the mixture was diluted with CH2Cl2 (50 mL) and extracted with saturated aqueous ammonium chloride (2×50 mL). The organic layer was washed with saturated aqueous sodium bicarbonate (50 mL) and brine (50 mL), dried over MgSO4, filtered and concentrated. The residue was purified by silica gel chromatography eluting with a gradient of 0-100% ethyl acetate in heptane to afford the title compound as white solid. MS m/z 438.74 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063065B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-80b3cf09d61542f6a633d5611988aaf2 |
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| Source note | uspto-grants-2011_11 |
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