HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753022Generated: October 28, 2026
3-(Trifluoromethyl)benzeneacetic acid → HCID 90093647, compound
https://huagongshe.com/reaction/1753022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)benzeneacetic acid | HCID 67695 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | HCID 90092825 | HCID 90092825 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90093647 | HCID 90093647 | 87% |
Reaction Steps
To a solution of (5-amino-pyridin-3-yl)-{1-[2-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-ethyl]-7-fluoro-1H-pyrrolo[3,2-c]pyridin-3-yl}-methanone (Preparation 29, 35 mg, 79 μmol), (3-trifluoromethyl-phenyl)-acetic acid (21.8 mg, 106 μmol) and DIPEA (48.94 μL, 277 μmol) in THF (3 mL), T3P (160 μL, 277 μmol) was added and the mixture stirred at 25° C. for 18 hours. The reaction was evaporated under reduced pressure, the residue partitioned between water and ethyl acetate, the organic extracts washed with saturated sodium bicarbonate solution, dried over sodium sulphate, evaporated in vacuo and triturated with pentane-ether to afford the title compound as a white solid (87%, 43 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163021B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-fc1e320da3be4063b6159ec0a3371a36 |
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| Source note | uspto-grants-2015_10 |
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