HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093513Generated: October 28, 2026
Trifluoroacetic acid → HCID 57708327, compound
https://huagongshe.com/reaction/2093513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57708276 | HCID 57708276 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57708327 | HCID 57708327 | 81.4% |
Reaction Steps
To a stirred solution of tert-butyl 3-(6-(4-phenoxyphenylamino)pyrimidin-4-ylamino)piperidine-1-carboxylate (110 mg, 0.238 mmol) in dry CH2Cl2 (1.0 mL) at 0° C. was added CF3COOH (0.5 mL, 5 vol) and the reaction mixture was kept at this temperature for 30 min. It was allowed to come to rt and to stir at this temperature for 3 h. The reaction mixture was concentrated under reduced pressure and the residue was quenched with water (2 mL), was basified with NaHCO3 solution, and was extracted with ethyl acetate (2×8 mL). The combined ethyl acetate extract was washed with water (2 mL), brine (2 mL), dried over Na2SO4 and concentrated under reduced pressure to give N4-(4-phenoxyphenyl)-N6-(piperidin-3-yl)pyrimidine-4,6-diamine (0.07 g, 81%) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445498B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-cf0694b4f2784ab6acda537be4d050cf |
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| Source note | uspto-grants-2013_05 |
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