HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 422992Erstellt: 25. Oktober 2026
Trifluoroacetic acid → 4-amino-N-(3-amino-1-(4-chlorophenyl)propyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide
https://huagongshe.com/reaction/422992
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | tert-butyl 4-(3-amino-1-(4-chlorophenyl)propylcarbamoyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidin-4-ylcarbamate | HCID 57750385 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-amino-N-(3-amino-1-(4-chlorophenyl)propyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide | HCID 57750335 | — |
Reaktionsschritte
Trifluoroacetic acid (0.05 mL) was added to a stirred suspension of tert-butyl 4-(3-amino-1-(4-chlorophenyl)propylcarbamoyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidin-4-ylcarbamate (Intermediate 38) (7.0 mg) in DCM (1 mL) under argon at 25° C. The resulting suspension was stirred at 25° C. for 2 days. The reaction mixture was evaporated to dryness to afford the di-TFA salt of 4-amino-N-(3-amino-1-(4-chlorophenyl)propyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide as a partially solid oil (13.0 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08101623B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-367d9b4511f64a9693164523efd0cf4e |
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| Quellennotiz | uspto-grants-2012_01 |
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