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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 485484생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/485484

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물BromineHCID 24408—
반응물Diethyl N-(4-aminobenzoyl)-L-glutamateHCID 73002—
반응물2,4-Diamino-6-(hydroxymethyl)pyrido[2,3-d]pyrimidineHCID 487416—
용매DimethylacetamideHCID 31374—
생성물Diethyl N-[4-[(2,4-diaminopyrido[2,3-d]pyrimidin-6-yl)methylamino]benzoyl]-L-glutamateHCID 12908481—

반응 조건

온도0 °C

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04536575
출처 데이터셋uspto-grants-1985_08
ORD IDord-2b14405cbfd5429bb28879b74d5a3181
출처 메모uspto-grants-1985_08