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HRID 559299作成日:2026年10月25日

Triphenylphosphine → 2-{(S)-1-[(3R,4S)-1-benzyl-4-(4-chloro-3-fluoro-phenyl)-pyrrolidin-3-yl]-ethoxy}-5-chloro-pyridine

https://huagongshe.com/reaction/559299

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Dibenzyl azodicarboxylateHCID 5387121—
反応物(R)-1-[(3R,4S)-1-benzyl-4-(4-chloro-3-fluoro-phenyl)-pyrrolidin-3-yl]-ethanolHCID 66999243—
反応物5-chloropyridin-2-olHCID 178516064—
溶媒TetrahydrofuranHCID 8028—
生成物2-{(S)-1-[(3R,4S)-1-benzyl-4-(4-chloro-3-fluoro-phenyl)-pyrrolidin-3-yl]-ethoxy}-5-chloro-pyridineHCID 6699920275%

反応手順

To a suspension of PPh3 (PPh3 polymer bound, 3 mmol PPh3/g resin) (216 mg, 0.65 mmol) in THF (10 mL) at 0° C. were added 5-chloro-pyridin-2-ol (58 mg, 0.45 mmol) and then DBAD (110 mg, 0.48 mmol). After 5 minutes was added (R)-1-[(3R,4S)-1-benzyl-4-(4-chloro-3-fluoro-phenyl)-pyrrolidin-3-yl]-ethanol (100 mg, 0.30 mmol). The reaction mixture was stirred over night at RT, filtered on celite and concentrated under vacuo. Extraction with EtOAc/aq.NaOH 1M, followed by column chromatography (SiO2, EtOAc/H, 1:3) yielded 100 mg (75%) of the title compound as a colorless oil. ES-MS m/e: 445.1 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063075B2
出典データセットuspto-grants-2011_11
ORD IDord-9563634efdfe483a977642a952ca4d64
出典メモuspto-grants-2011_11