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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1263476생성일: 2026년 10월 25일

Thionyl Chloride → N1-(S-(4-methoxybenzyl) thiosalicyloyl)-N4-methylpiperazine

https://huagongshe.com/reaction/1263476

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물1-MethylpiperazineHCID 53167—
반응물Benzoic acid, 2-[[(4-methoxyphenyl)methyl]thio]-HCID 3568003—
반응물2-[(Phenylmethyl)thio]benzoyl chlorideHCID 20067340—
용매BenzeneHCID 241—
용매WaterHCID 962—
생성물N1-(S-(4-methoxybenzyl) thiosalicyloyl)-N4-methylpiperazineHCID 69733570—

반응 단계

The compound N1-(S-(4-methoxybenzyl) thiosalicyloyl)-N4-methylpiperazine (compound 2) was prepared in a manner similar to that described above for S-(4-methoxybenzyl)-N-(2-(N′,N′-dimethylamino)ethyl) thiosalicylamide. After preparing the S-benzylthiosalicyloyl chloride from 0.02M(5.487 g) of S-(4-methoxybenzyl)thiosalicylic acid and 20 mL of SOCl2, the mixture was suspended in warm benzene (30 mL) and was slowly added to a 20 mL cold solution of 4.007 g(0.04M) 1-methylpiperazine in benzene. The mixture was stirred overnight at room temperature. The next day 40 mL of water were added, the aqueous layer was separated, and extracted twice with 15 mL CH2Cl2. The extracts were combined with the benzene layer, washed with 10% NaOH solution and dried over anhydrous MgSO4. Removal of the solvents under reduced pressure left an oily product which was dissolved in petroleum ether (10 ml). A precipitate separated out upon cooling in an ice bath. The separated solid was collected by suction filtration and washed with petroleum ether to give 3.372 g(47%) of the product in the form of white crystals and having a melting point of 77-78° C. and the following specifications:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06541479B1
출처 데이터셋uspto-grants-2003_04
ORD IDord-3834619c89ec4b82ae456e520aef33d7
출처 메모uspto-grants-2003_04