HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430816Generated: November 1, 2026
Trifluoroacetic acid → HCID 131732379, compound
https://huagongshe.com/reaction/1430816
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131732377 | HCID 131732377 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131732379 | HCID 131732379 | 79.3% |
Reaction Steps
Methyl ((3R,4R)-1-(2-chloro-5-cyano-3-(N-Boc-amino)phenyl)-3-((triisopropylsilyl)oxy)piperidin-4-yl)carbamate (242 mg, 0.354 mmol) was treated with TFA (25% in 1,2-dichloroethane, 4 mL, 12.98 mmol) at room temperature for 1 h. The reaction mixture was diluted with dichloromethane and washed with cold saturated sodium bicarbonate/1N aqueous sodium hydroxide (pH 10), the organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo, the crude product was purified by flash chromatography on silica gel using an automated ISCO system (40 g column, eluting with 0-20% ethyl acetate/dichloromethane). Methyl ((3R,4R)-1-(3-amino-2-chloro-5-cyanophenyl)-3-((triisopropylsilyl)oxy)piperidin-4-yl)carbamate (135 mg) was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940736B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-8713f9f72e4b43159cce149aff3197e8 |
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| Source note | uspto-grants-2015_01 |
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