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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370522Erstellt: 24. Oktober 2026

Triphenylphosphine → Diethyl N-[4-[(2,4-diaminopyrido[2,3-d]pyrimidin-6-yl)methylamino]benzoyl]-L-glutamate

https://huagongshe.com/de/reaction/370522

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktBromineHCID 24408—
EduktDiethyl N-(4-aminobenzoyl)-L-glutamateHCID 73002—
Edukt2,4-Diamino-6-(hydroxymethyl)pyrido[2,3-d]pyrimidineHCID 487416—
LösungsmittelDimethylacetamideHCID 31374—
ProduktDiethyl N-[4-[(2,4-diaminopyrido[2,3-d]pyrimidin-6-yl)methylamino]benzoyl]-L-glutamateHCID 12908481—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of triphenylphosphine (430 mg, 1.64 mmol) in anhydrous DMAC (4 ml) at 0° C. was treated dropwise under N2 with bromine (84 μL, 1.64 mmol). The solution was stirred at 0° C. for 15 minutes, treated with the compound obtained in Example 2 (100 mg, 0.76 mmol), and stirred at 25° C. for 1.7 hours to give the compound of Formula IIIA. This solution was treated with diethyl p-aminobenzoyl-L-glutamate (194 mg, 0.603 mmol), stirred at 25° C. for 17 hours and poured into ice water (40 ml). The resulting solution (pH 2) was filtered to remove triphenylphosphine oxide, adjusted to pH 6.8 with 50% NaOH, and cooled in an ice bath. The precipitate of crude product (VII; R=H, R1 =C2H5) was collected by centrifugation, washed with H2O and dried in vacuo (P2O5); yield 136 mg (73%). The retention time (HPLC) and rf value (TLC) of this product were identical to those obtained from the analytical sample obtained in Part A of this example. Mass spectrum: m/e 496 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04526964
Quelldatensatzuspto-grants-1985_07
ORD IDord-fbcac3e64fe642baba4a087245e81abd
Quellennotizuspto-grants-1985_07