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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259396생성일: 2026년 10월 23일

Hexamethylphosphoramide → Benzhydryl 7-(2-thienylacetamido)-3-(4-hydroxybutanoyloxymethyl)-2-cephem-4-carboxylate

https://huagongshe.com/ko/reaction/259396

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물Sodium OxybateHCID 23663870—
반응물Benzhydryl 7-(2-thienylacetamido)-3-bromomethyl-3-cephem-4-carboxylateHCID 70634766—
용매Ethyl AcetateHCID 8857—
생성물Benzhydryl 7-(2-thienylacetamido)-3-(4-hydroxybutanoyloxymethyl)-2-cephem-4-carboxylateHCID 131710853—

반응 단계

To a solution of 2.24 g. (3.8 mmol) of benzhydryl 7-(2-thienylacetamido)-3-bromomethyl-3-cephem-4-carboxylate in 20 ml. of hexamethylphosphoramide (HMPA) at 0° C. under nitrogen was added a suspension of 0.530 g. (4.2 mmol) of sodium 4-hydroxybutanoate in 25 ml. of HMPA. After stirring 1.5 hours, ethyl acetate was added, and the resulting solution was washed with water (5X) and brine and dried over anhydrous MgSO4. Evaporation in vacuo to dryness provided 2.12 g. of product which was combined with that of an identical reaction ran on a 1 mmol scale. The combined products were chromatographed on a silica gel column using a cyclohexane:ethyl acetate (1:2) eluant to provide 293 mg. of a mixture of the title product and the corresponding 3-cephem compound. For the title product: nmr (CDCl3) δ1.7-2.6 ##STR26## 3.55 (m, 2, CH2OH), 3.83 (s, 2, side chain CH2), 4.63 (bs, 1, --CH2OH), 5.0 (s, 1, C4 --H), 5.23 (d, 1, J = 4 Hz, C6 --H), 5.58 (dd, 1, J = 4 and 8 Hz, C7 --H), 6.42 (bs, 1, C2 --H), 6.95 (s, 1, ester CH), and 7.36 (m, 13, thienyl + ArH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04038275
출처 데이터셋uspto-grants-1977_07
ORD IDord-eaf780383c304188828ec1b9c6543e33
출처 메모uspto-grants-1977_07