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HRID 1255521作成日:2026年10月24日

Potassium bisulfate → (4R)-4-{[6-(Benzyloxy)pyridin-2-yl]oxy}-1-(tert-butoxycarbonyl)-L-proline

https://huagongshe.com/ja/reaction/1255521

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium bisulfateHCID 516920—
反応物1-(1,1-Dimethylethyl) (2S)-4-hydroxy-1,2-pyrrolidinedicarboxylateHCID 11138980—
反応物Potassium tert-butoxideHCID 23665647—
反応物2-(Benzyloxy)-6-fluoropyridineHCID 57753871—
溶媒Dimethyl SulfoxideHCID 679—
生成物(4R)-4-{[6-(Benzyloxy)pyridin-2-yl]oxy}-1-(tert-butoxycarbonyl)-L-prolineHCID 58158006100%

反応手順

A 500 mL 3-neck round bottom flask under nitrogen was charged with Boc-L-4-hydroxyproline (Chem Impex) (2.00 g, 8.65 mmol) and DMSO (80 ml). Attached an addition funnel containing a solution of the product of Step 1 (1.758 g, 8.65 mmol) in DMSO (10 ml). Cooled reaction in an ice bath to +18° C. Added potassium-t-butoxide (2.91 g, 25.9 mmol) slowly keeping the internal temperature<20° C. Stirred 45 minutes at room temperature. Cooled to 15° C. Added contents of addition funnel dropwise. Warmed to room temperature. Stirred 1.5 hours. Poured into 2.5% potassium bisulfate. Extracted three times with ethyl acetate, washed combined organic portions with water then brine, dried with anhydrous magnesium sulfate, filtered and rotary evaporated filtrate to give the title compound as a white foam. (3.58 g, 8.65 mmol, 100% yield). LCMS (ES+) m/z 415.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08461107B2
出典データセットuspto-grants-2013_06
ORD IDord-06acae8a1b5a4158b3f7d4b686e66eae
出典メモuspto-grants-2013_06