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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 246866생성일: 2026년 10월 26일

Peracetic Acid → 3[2-(4-Ethyl-2,3-dioxopiperazine-1-carbonylamino)-2-phenylacetamido]-4-methyl-3-methylsulphinylazetidin-2-one

https://huagongshe.com/reaction/246866

반응식

참여 물질

역할이름HCID투입량
반응물Peracetic AcidHCID 6585—
반응물3[2-(4-Ethyl-2,3-dioxopiperazine-1-carbonylamino)-2-phenylacetamido]-4-methyl-3-methylthioazetidin-2-oneHCID 20162866—
용매Acetic AcidHCID 176—
용매1,4-DioxaneHCID 31275—
생성물3[2-(4-Ethyl-2,3-dioxopiperazine-1-carbonylamino)-2-phenylacetamido]-4-methyl-3-methylsulphinylazetidin-2-oneHCID 20162853—

반응 단계

The azetidinone (60) (250 mg) in dry dioxan (10 ml) was treated with a (5.07% w/v) solution of peracetic acid in acetic acid (0.69 ml) for 1.5 hour. The solvent was then evaporated in vacuo, the complete removal of acidic residues being ensured. Silica gel chromatography of the residue gave the title compound as a pale--white solid (149 mg), νmax. (Nujol) 3300, 1760, 1710, and 1670 cm-1, δ[(CD3)2SO]0.65, 0.93, 1.16 and 1.19 (each d, J 6.4 Hz, together 3H), (1.07 (t, J 7 Hz, 3H), 1.99, 2.14, 2.39, 2.64 and 2.68 (each s, together 3H), 3.37 (q, J 7 Hz, 2H), 3.47-3.52 (m, 2H), 3.179-3.92 (m, 2H), 3.92-4.10 (complex m, together 1H), [5.45-5.60 (complex m) and 5.86 (d, J 7 Hz), together 1H], 7.27-7.55 (m, 5H), 8.63 and 8.74 br (each s, together 1H, exch), 9.14 and 9.35 br (each s, together 1H, exch.) and 9.65-10.00 (complex m, together 1H, exch).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04704385
출처 데이터셋uspto-grants-1987_11
ORD IDord-705f4981fefa4c3ba716638b5401e372
출처 메모uspto-grants-1987_11