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HRID 60241作成日:2026年10月25日

Beta-Propiolactone → tert-Butyl 1-(oxetan-3-yl)piperidin-4-yl carbamate

https://huagongshe.com/reaction/60241

反応式

関与物質

役割名称HCID仕込み量
反応物Beta-PropiolactoneHCID 2365—
反応物4-(N-Boc-amino)piperidineHCID 723833—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
生成物tert-Butyl 1-(oxetan-3-yl)piperidin-4-yl carbamateHCID 5660452867%

反応手順

To a suspension of piperidin-4-yl-carbamic acid tert-butyl ester (200 mg, 1.0 mmol) in DCE (6 mL) was added oxetanone (60 mg, 0.83 mmol) in DCE (2 mL). After 75 min, sodium triacetoxyborohydride (282 mg, 1.33 mmol) was added in one portion. After 20 hours at ambient temperature, the reaction mixture was loaded directly onto a 5 g SCX-2 cartridge which was washed with methanol, then 2N ammonia in methanol. Concentration of the combined basic fractions in-vacuo followed by flash chromatography of the resultant residue (silica, 5 g column, Si-SPE, 0-10% methanol in dichloromethane) afforded the title compound as a white solid (141 mg, 67%). 1H NMR (300 MHz, CDCl3): 4.62-4.61 (m, 4H), 4.44 (s, 1H), 3.46-3.45 (m, 2H), 2.67 (d, J=10.9 Hz, 2H), 2.02-1.88 (m, 4H), 1.44 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440976B2
出典データセットuspto-grants-2016_09
ORD IDord-21ed99da9d1943258608cfc03367be3a
出典メモuspto-grants-2016_09