HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409475Generated: October 29, 2026
Trifluoroacetic acid → HCID 59614335, compound
https://huagongshe.com/reaction/409475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 42633526 | HCID 42633526 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59614335 | HCID 59614335 | — |
Reaction Steps
To a solution of (2R,4S)-4-{(3,5-Bis-trifluoromethyl-benzyl)-[5-(1-methyl-1H-pyrazol-4-yl)-pyrimidin-2-yl]-amino}-2-ethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1.2 g, 2 mmol) in CH2Cl2 (20 mL) is added trifluoroacetic acid (7 mL) at room temperature. The reaction mixture is stirred at room temperature for 1.5 hours. The mixture is quenched with saturated aqueous NaHCO3 solution, then extracted with CH2Cl2. The combined organic layer is washed by saturated aqueous NaHCO3 solution, then dried over Na2SO4 and concentrated under reduced pressure to give (3,5-bis-trifluoromethyl-benzyl)-((3S,5R)-5-ethyl-pyrrolidin-3-yl)-[5-(1-methyl-1H-pyrazol-4-yl)-pyrimidin-2-yl]-amine as a yellow oil (1.01 g, quant.). ESI-MS m/z: 499 [M+1]+, Retention time 1.84 min (condition A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759365B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-45cafba5e37e448d804e5f837070ff6f |
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| Source note | uspto-grants-2014_06 |
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