HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571822Generated: October 30, 2026
Trifluoroacetic acid → HCID 71086659, compound
https://huagongshe.com/reaction/571822
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86674684 | HCID 86674684 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 71086659 | HCID 71086659 | 72% |
Reaction Steps
To a stirred solution of trifluoroacetic acid (225 μl) in water (4.5 ml) was added a solution of tert-butyl (RS)-2-(3-chloro-4-(3-(3-cyanophenyl)ureido)phenyl)morpholine-4-carboxylate (114 mg) in acetonitrile (2 ml). The reaction mixture was then capped and the mixture was shaken at 80° C. for 3 h. The reaction mixture was then cooled to room temperature and poured into 1 M aq. NaOH and the resulting mixture was extracted twice with EtOAc. The organic layers were dried over Na2SO4 and concentrated in vacuo. The crude material was purified by flash column chromatography (Isolute® Flash-NH2 from Separtis); gradient: heptane/EtOAc/MeOH) to afford (RS)-1-(2-chloro-4-(morpholin-2-yl)phenyl)-3-(3-cyanophenyl)urea (58 mg, 72%) as a white solid. MS (ISP): 359.1 ([{37Cl}M+H]+), 357.1 ([{35Cl}M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029370B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-d6d6bc2d360f444fa38ec006a16a7c0f |
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| Source note | uspto-grants-2015_05 |
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