HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929167Generated: October 30, 2026
Trifluoroacetic acid → HCID 90067498, compound
https://huagongshe.com/reaction/929167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 89558611 | HCID 89558611 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90067498 | HCID 90067498 | — |
Reaction Steps
To a stirred solution of tert-butyl 4-((4-(2-(((3R,3aR,6R,6aS)-6-((tert-butyldimethylsilyl)oxy)hexahydrofuro[3,2-b]furan-3-yl)oxy)-6-chloro-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazo[4,5-b]pyridin-5-yl)phenyl)ethynyl)piperidine-1-carboxylate (147 mg, 0.178 mmol) in anhydrous DCM (2.0 mL) at room temperature was added trifluoroacetic acid (0.2 mL). The reaction was stirred for 2 h at room temperature, and then poured into saturated aqueous sodium bicarbonate (40 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic layers were dried over sodium sulfate, and then concentrated under reduced pressure to afford the title compound as a colorless oil. LC-MS: calculated for C37H53ClN4O5Si2 724.32 observed m/e: 725.32 (M+H)+ (Rt 2.56/4 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290517B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f028798d8a944da8b2dc3238e2cf7208 |
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| Source note | uspto-grants-2016_03 |
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