HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68682Erstellt: 25. Oktober 2026
Diisopropylethylamine → tert-butyl 3-(3-(3-(methylthio)-1-phenyl-1H-indazol-6-yl)ureido)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/68682
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Triphosgene | HCID 94429 | — |
| Edukt | 1-Boc-3-aminopyrrolidine | HCID 2756370 | — |
| Edukt | 3-(methylthio)-1-phenyl-1H-indazol-6-amine | HCID 49839977 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | tert-butyl 3-(3-(3-(methylthio)-1-phenyl-1H-indazol-6-yl)ureido)pyrrolidine-1-carboxylate | HCID 67448228 | — |
Reaktionsschritte
Into a 50-mL 3-necked round-bottom flask, was placed a solution of bis(trichloromethyl)carbonate (200 mg, 0.67 mmol) in dichloromethane (3 mL). To the resulting mixture was then added a mixture of 3-(methylthio)-1-phenyl-1H-indazol-6-amine (500 mg, 1.96 mmol, 1.00 equiv) and DIEA (560 mg, 4.33 mmol, 2.21 equiv) in dichloromethane (2 mL) dropwise with stirring at 0° C. in 30 min. The resulting solution was stirred for 3 h at 15° C. The resulting mixture was added to a solution of tert-butyl 3-aminopyrrolidine-1-carboxylate (440 mg, 2.37 mmol, 1.21 equiv) in dichloromethane (3 mL) dropwise with stirring at 15° C. in 15 min. The resulting solution stirred for an additional 4 h at 15° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate:petroleum ether (1:4˜1:3) to yield tert-butyl 3-(3-(3-(methylthio)-1-phenyl-1H-indazol-6-yl)ureido)pyrrolidine-1-carboxylate as a white solid. MS: 468 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822447B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-64c5866a5fbc4a87a594f9858b5d8e92 |
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| Quellennotiz | uspto-grants-2014_09 |
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