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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1709375생성일: 2026년 10월 23일

Triethylamine → HCID 178514123, 화합물

https://huagongshe.com/ko/reaction/1709375

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물CarumonamHCID 6540466—
반응물Sodium 2-ethylhexanoateHCID 23672331—
용매AcetoneHCID 180—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물HCID 178514123HCID 17851412390.5%

반응 단계

110 g (0.235 mol) of crude (3S,4S)-3-[(Z)-2-(2-amino-4-thiazolyl)-2-[(carboxymethoxy)imino]acetamido]-4-carbamoyloxymethyl-2-oxo-1-azetidinesulphonic acid (obtained according to Example 41) are dispersed in 4.7 l of methanol and treated with 72.3 ml (0.518 mol) of triethylamine and 282.9 ml (0.566 mol) of a 2N solution of sodium 2-ethylcaproate in ethyl acetate. The solution obtained is stirred for 10 minutes, diluted with 9 l of acetone and concentrated to 3 l. The residual suspension is diluted with 3 l of acetone, filtered and the crystalline salt is washed with ether and dried. 108.59 g (90.5%) of (3S,4S)-3-[(Z)-2-(2-amino-4-thiazolyl)-2-[(carboxymethoxy)-imino]acetamido]-4-carbamoyloxymethyl-2-oxo-1-azetidinesulphonic acid disodium salt are obtained. This crude salt is dissolved in 420 ml of water. 1050 ml of ethanol are added thereto and subsequently (after a few minutes) a further 210 ml of ethanol are added. The solution is turbid and is stirred for 1 hour. 1770 ml of ethanol are now added dropwise thereto within 2 hours. After stirring for a further 1 hour and cooling to 0° C., the precipitate is filtered off and washed with ethanol. The crystals obtained are dispersed in 170 ml of ethanol and 680 ml of ether, filtered off and washed with ether. After drying under greatly reduced pressure at 40° C., there obtained 102.9 g (85.5%) of (3S,4S)-3-[(Z)-2-(2-amino-4-thiazolyl)-2-[(carboxymethoxy)imino]acetamido]-4-carbamoyloxymethyl-2-oxo-1-azetidinesulphonic acid disodium salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04948898
출처 데이터셋uspto-grants-1990_08
ORD IDord-8ed6fac4d3a048cfa3a08018758bba27
출처 메모uspto-grants-1990_08