HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367286Generated: November 1, 2026
Trifluoroacetic acid → HCID 15982220, compound
https://huagongshe.com/reaction/1367286
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 66970774 | HCID 66970774 | — |
| Reactant | HCID 66971161 | HCID 66971161 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15982220 | HCID 15982220 | — |
Reaction Steps
The combined materials of {5-[Hydroxy-(1H-pyrrolo[2,3-b]-pyridin-3-yl)-methyl]-6-methyl-pyridin-2-yl}-(4-trifluoromethyl-benzyl)-carbamic acid tert-butyl ester (37) and {5-[Methoxy-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methyl]-6-methyl-pyridin-2-yl }-(4-trifluoromethyl-benzyl)-carbamic acid tert-butyl ester (38) (194 mg, 0.378 mmol) were dissolved in acetonitrile (3 mL) and triethylsilane (0.30 mL, 1.9 mmol) and trifluoroacetic acid (0.17 mL, 2.3 mmol) were added. After stirring at 25° C. for overnight, TLC analysis indicated that the reaction was about 50% complete. To the reaction mixture was added triethylsilane (0.30 mL, 1.9 mmol), and trifluoroacetic acid (0.17 mL, 2.3 mmol). The mixture was allowed to stir for another 48 hours at 25° C. and the solvent, excess triethylsilane and trifluoroacetic acid were removed by evaporation. Ethyl acetate was added and washed with saturated sodium bicarbonate. The organic layer was dried over magnesium sulfate, filtered and concentrated at reduced pressure to afford a brown oil. Purification of 80 mg of the crude material was carried out using preparatory chromatography (50% ethyl acetate in hexanes) to afford the compound as an off-white solid (P-0013, 10 mg, 0.025 mmol). MS(ESI) [M+H+]+=397.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893075B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-f557a00ee7d04c2aaae1bc48df0de500 |
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| Source note | uspto-grants-2011_02 |
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