HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990891Generated: October 29, 2026
Trifluoroacetic acid → HCID 58706342, compound
https://huagongshe.com/reaction/1990891
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 66912254 | HCID 66912254 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58706342 | HCID 58706342 | 93.1% |
Reaction Steps
To a solution of 4-(5-cyano-benzooxazol-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (6.62 g, 19.33 mmol, 1.0 equiv) in dichloromethane (100 mL) was added trifluoro-acetic acid (7.4 mL, 11.03 g, 96.7 mmol, 5.0 equiv). After stirring under Ar at rt for 18 h excess trifluoro-acetic acid was removed under reduced pressure and the crude solid taken up in dichloromethane (100 mL) and water (100 mL). The pH was adjusted to 10 by addition of a conc. solution of K2CO3 and the solution extracted with dichloromethane/2-propanol (4:1, 3×50 mL). The combined organic phases were dried over MgSO4, the organic solvent evaporated under reduced pressure and the crude reaction product purified with column chromatography on silica eluting with a gradient of dichloromethane/methanol (100:0→95:5) containing 33% of NH4OH to yield 4.36 g (93%) of the title compound. MS (ESI): 243.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645753B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-84a14a5e4b664b459b2c034fb3e83574 |
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| Source note | uspto-grants-2010_01 |
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