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HRID 1255086作成日:2026年10月25日

Triphenylphosphine → (R)-((R)-quinuclidin-3-yl) 2-(4-fluorophenylamino)-2-phenylacetate

https://huagongshe.com/reaction/1255086

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-Quinuclidinol, (+)-HCID 736411—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物(R)-(4-fluoro-phenylamino)-phenyl-acetic acidHCID 7006576—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-((R)-quinuclidin-3-yl) 2-(4-fluorophenylamino)-2-phenylacetateHCID 5940113379.2%

反応手順

To a solution of (R)-(4-fluoro-phenylamino)-phenyl-acetic acid (I253) (420 mg, 1.71 mmol) in dry THF (40 mL), are sequentially added (S)-quinuclidin-3-ol (218 mg, 1.71 mmol), DEAD (407 ul, 2.57 mmol) and triphenylphosphine (674 mg, 2.57 mmol). The reaction is refluxed for 30 minutes under N2 flowstream and then the solvent is evaporated. The residue is partitioned between water and EtOAc, the organic layer is separated, dried over Na2SO4, filtered and evaporated to dryness. The resulting crude is purified by flash chromatography (DCM/MeOH=95/5) to obtain the title compound as a pale yellow oil (480 mg, 79% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08455646B2
出典データセットuspto-grants-2013_06
ORD IDord-9bc76f026041427d85a93ef3e5255325
出典メモuspto-grants-2013_06