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HRID 82245Erstellt: 24. Oktober 2026

(alpha,alpha,alpha-Trifluoro-4-tolyl)acetic acid → HCID 178455449, Verbindung

https://huagongshe.com/de/reaction/82245

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(alpha,alpha,alpha-Trifluoro-4-tolyl)acetic acidHCID 118342—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
EduktHCID 178455448HCID 178455448—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium BicarbonateHCID 516892—
ProduktHCID 178455449HCID 17845544992%

Reaktionsbedingungen

Temperatur50 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846698B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-f3606333d59744beab7c49d3b5162430
Quellennotizuspto-grants-2014_09