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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38258생성일: 2026년 10월 24일

Hydrochloric Acid → [3-Chloro-2-[[4-[(4-chlorophenyl)acetyl]-1-piperazinyl]-methyl]-phenoxy]-acetic Acid

https://huagongshe.com/ko/reaction/38258

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물Sodium HydroxideHCID 14798—
반응물3-Chlorophenylacetic acidHCID 15879—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물[4-chloro-2-[4-(phenylsulfonyl)-1-piperazinylmethyl]phenoxy]-acetic AcidHCID 53317503—
용매DimethylformamideHCID 6228—
생성물[3-Chloro-2-[[4-[(4-chlorophenyl)acetyl]-1-piperazinyl]-methyl]-phenoxy]-acetic AcidHCID 11561177—

반응 단계

The product from Example 11 part (a) (300 mg) was dissolved in DMF (10 ml) and treated with HATU ((570 mg), followed by 3-chlorobenzeneacetic acid (190 mg). The reaction mixture was stirred for 18 h, treated with 1M NaOH (3 ml) and stirred for 3 h. The reaction was acidified with 2M HCl, diluted with ethyl acetate, washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by RPHPLC to give the title compound (110 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524715B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-78899de241734231a9ed10a9819cd875
출처 메모uspto-grants-2013_09