HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 82245Erstellt: 24. Oktober 2026
(alpha,alpha,alpha-Trifluoro-4-tolyl)acetic acid → HCID 178455449, Verbindung
https://huagongshe.com/de/reaction/82245
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (alpha,alpha,alpha-Trifluoro-4-tolyl)acetic acid | HCID 118342 | — |
| Edukt | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Edukt | HCID 178455448 | HCID 178455448 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Sodium Bicarbonate | HCID 516892 | — |
| Produkt | HCID 178455449 | HCID 178455449 | 92% |
Reaktionsschritte
(5-Amino-pyridin-3-yl)-{7-[3-(tert-butyl-dimethyl-silanyloxymethyl)-oxetan-3-yl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}-methanone (Preparation 216, 30 mg, 0.068 mmol) was dissolved in dry pyridine (2 mL) under nitrogen and to this was added (4-trifluoromethyl-phenyl)-acetic acid (21 mg, 0.102 mmol), followed by HATU (39 mg, 0.102 mmol). The reaction mixture was heated to 50° C. and stirred overnight. The reaction was then cooled to room temperature, diluted with dichloromethane (5 mL) and saturated aqueous sodium bicarbonate was added (5 mL). The phases were separated and the aqueous layer was extracted with dichloromethane (3×5 mL). The combined organics were concentrated to dryness to afford N-(5-{7-[3-(tert-butyl-dimethyl-silanyloxymethyl)-oxetan-3-yl]-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl}-pyridin-3-yl)-2-(4-trifluoromethyl-phenyl)-acetamide as a pale yellow solid 39 mg, 92% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846698B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-f3606333d59744beab7c49d3b5162430 |
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| Quellennotiz | uspto-grants-2014_09 |
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