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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1435331Erstellt: 25. Oktober 2026

4-Methylmorpholine → 4-[4-Amino-5-(2,3-difluoro-6-methoxy-benzoyl)-pyrimidin-2-ylamino]-piperidine-1-sulfonic Acid acetyl-amide

https://huagongshe.com/reaction/1435331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
Edukt2-DimethylaminopyridineHCID 21885—
Edukt4-[4-Amino-5-(2,3-difluoro-6-methoxy-benzoyl)-pyrimidin-2-ylamino]-piperidine-1-sulfonic acid amideHCID 10072033—
KatalysatorAcetic AnhydrideHCID 7918—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[4-Amino-5-(2,3-difluoro-6-methoxy-benzoyl)-pyrimidin-2-ylamino]-piperidine-1-sulfonic Acid acetyl-amideHCID 10480467—

Reaktionsschritte

4-[4-Amino-5-(2,3-difluoro-6-methoxy-benzoyl)-pyrimidin-2-ylamino]-piperidine-1-sulfonic acid amide (50 mg, Example 285) in dichloromethane (10 mL), N-methyl morpholine (0.1 mL, Aldrich) and dimethylaminopyridine (1 mg, Aldrich) was chilled in ice and added acetic anhydride (5 drops). The mixture was stirred cold for two hours and quenched with methanol. The mixture was evaporated to dryness and chromatographed on silica gel (dichloromethane, then ethyl acetate). Fractions corresponding to product were combined and crystallized from dichloromethane/ethyl ether to give 45 mg of colorless material, MP 153° C. (dec). MS(ES) MH+485

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07615634B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-396eb26058e64e3693d3fafce2f0163e
Quellennotizuspto-grants-2009_11