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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128594생성일: 2026년 10월 26일

Ethanesulfonylchloride, 2-chloro- → 1-(2-Methoxy-4-(1-ethenylsulfonyl-4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)piperazine-2-carboxamide

https://huagongshe.com/reaction/128594

반응식

참여 물질

역할이름HCID투입량
반응물Ethanesulfonylchloride, 2-chloro-HCID 15385—
반응물DiisopropylethylamineHCID 81531—
반응물1-(2-Methoxy-4-(4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)piperazine-2-carboxamide dihydrochlorideHCID 67656469—
용매DichloromethaneHCID 6344—
생성물1-(2-Methoxy-4-(1-ethenylsulfonyl-4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)piperazine-2-carboxamideHCID 18914163—

반응 단계

2-Chloroethanesulfonyl chloride (0.035 ml, 54.6 mg, 0.33 mmol) in methylene chloride (3 ml) was cooled in an ice bath under nitrogen. A solution of 1-(2-methoxy-4-(4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)-piperazine-2-carboxamide dihydrochloride (149 mg, 0.28 mmol) and diisopropylethylamine (0.243 ml, 0.18 g, 1.4 mmol) in methylene chloride (3 ml) was added dropwise and the mixture was stirred in the cold for 18 hours. The mixture was concentrated in vacuo and the residue chromatographed on silica gel eluted with 3% methanol in methylene chloride. The combined product fractions were evaporated to dryness in vacuo to give 1-(2-methoxy-4-(1-ethenylsulfonyl-4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)piperazine-2-carboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464788
출처 데이터셋uspto-grants-1995_11
ORD IDord-377d1b3ed3b348be93c0c1e64baff28d
출처 메모uspto-grants-1995_11