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HRID 73021作成日:2026年10月24日

N-acetonyl-8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxamide → 4-Isopropoxy-3-methylbenzaldehyde

https://huagongshe.com/ja/reaction/73021

反応式

関与物質

役割名称HCID仕込み量
反応物N-acetonyl-8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxamideHCID 70872809—
溶媒TetrahydrofuranHCID 8028—
生成物4-Isopropoxy-3-methylbenzaldehydeHCID 50998243164%

反応条件

温度75 °C

反応手順

To N-acetonyl-8-benzyl-3-(4-isopropoxy-3-methyl-benzoyl)-11-oxa-3,8-diazaspiro[5.5]undecane-10-carboxamide (136 mg, 0.26 mmol) in THF (3 mL) was added Burgess' Salt (155 mg, 0.65 mmol) and the reaction mixture was heated at 75° C. in a sealed vial for 2 hours. The solvents were removed under reduced pressure, and the residue was dissolved in DMF (1 mL), filtered and purified by Waters preparative LC/MS (1-99% ACN/H2O (5 mM HCl)). The desired fractions were concentrated in vacuo and the residue partitioned between EtOAc/saturated aqueous NaHCO3 solution. The layers were separated and the aqueous layer was extracted with EtOAc (2×). The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to yield 8-benzyl-10-(5-methyloxazol-2-yl)-11-oxa-3,8-diazaspiro[5.5]undecan-3-yl]-(4-isopropoxy-3-methyl-phenyl)methanone (76 mg, 58%) as a foam. ESI-MS m/z calc. 503.6. Found 504.5 (M+1)+; Retention time: 1.74 minutes (3 min run).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828996B2
出典データセットuspto-grants-2014_09
ORD IDord-499a0e9ff92d40a482c4a7714ed2a2a1
出典メモuspto-grants-2014_09