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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 382639생성일: 2026년 10월 23일

Dichloromethane → Potassium (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-7-yl)-1-methyl-1-carbapen-2-em-3-carboxylate

https://huagongshe.com/ko/reaction/382639

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물TriphenylphosphineHCID 11776—
반응물Potassium 2-ethylhexanoateHCID 23669619—
반응물allyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-7-yl)-1-methyl-1-carbapen-2-em-3-carboxylateHCID 131722909—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Ethyl AcetateHCID 8857—
생성물Potassium (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-7-yl)-1-methyl-1-carbapen-2-em-3-carboxylateHCID 131722911—

반응 단계

To a solution of 117 mg of allyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-7-yl)-1-methyl-1-carbapen-2-em-3-carboxylate in a mixed solvent of 2.5 ml of dichloromethane and 2.5 ml of ethy acetate were added 8.1 mg of triphenylphosphine, 56.5 mg of potassium 2-ethylhexanoate, and 11.8 mg of tetrakis(triphenylphosphine)palladium (0), and the mixture was stirred under the atmosphere of argon at room temperature for 20 minutes. After confirming the exhaustion of the starting materials, the reaction mixture was diluted with 10 ml of ethyl acetate, extracted three or four times with water, and the aqueous layer was concentrated under reduced pressure. The concentrate was purified by column chromatography on COSMOSEAL 40C18-PREP to give the title compound in a yield of 55 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06310056B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-50feba7d8ec4461589af473598174060
출처 메모uspto-grants-2001_10