HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391980Generated: November 2, 2026
Trifluoroacetic acid → HCID 10369410, compound
https://huagongshe.com/reaction/1391980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 3-(Trifluoromethyl)phenyl isocyanate | HCID 9483 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69292175 | HCID 69292175 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10369410 | HCID 10369410 | — |
Reaction Steps
A solution of {(3S)-1-[(1S,2S)-(1-{[benzyloxycarbonyl-(2,4-dimethyl-benzyl)-amino]-methyl}-2-hydroxy-pent-3-ynyl)]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert-butyl ester (1.16 g, 1.74 mmol, see procedure 1c above) was dissolved in CH2Cl2 (16 mL) and treated with TFA (8 mL). The solution was stirred for 3 h and then concentrated in vacuo. The residue was dissolved in CH2Cl2 and concentrated in vacuo; this procedure was repeated. A portion (0.22 mmol) of the product amine was dissolved in CH2Cl2 (4 mL). The resultant solution was charged sequentially with N, N-diisopropylethylamine (0.16 mL, 0.88 mmol) and (meta-trifluoromethyl-phenyl)isocyanate (0.033 mL, 0.22 mmol). The reaction was stirred for 12 h and partitioned between EtOAc and sat. NH4Cl. The organic phase was washed with sat. NaHCO3 and brine, and then dried (Na2SO4), filtered, and concentrated in vacuo. The residue was dissolved in MeOH (6 mL). The resultant solution was charged with 5% Pd/C, Degussa style (50 mg), stirred under H2 (1 atm) for 12 h at RT, filtered, and concentrated in vacuo. The residue was purified by reverse-phase HPLC to afford the title compound as a white powder after lyopholization. MS found: (M+H)+=521.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07338975B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-eadec993166046db934d001690e7f113 |
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| Source note | uspto-grants-2008_03 |
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