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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133596생성일: 2026년 10월 26일

Chloroform → 1-(4-chlorobenzyl)-4-[[N-(3,5-bis(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine

https://huagongshe.com/reaction/133596

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물DichloromethaneHCID 6344—
반응물3,5-Bis(trifluoromethyl)benzoyl chlorideHCID 101856—
반응물1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidineHCID 18426155—
용매MethanolHCID 887—
생성물1-(4-chlorobenzyl)-4-[[N-(3,5-bis(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidineHCID 18426201—

반응 단계

A dichloromethane (1 mL) solution of 3,5-bis(trifluoromethyl)benzoyl chloride (0.058 mmol) was added to a mixture of 1-(4-chlorobenzyl)-4-[(glycylamino)methyl]piperidine (0.050 mmol) with chloroform (0.2 mL), a piperidinomethylpolystyrene (58 mg) and dichloromethane (0.75 mL). The resulting reaction mixture was stirred at room temperature for 2 hours, and methanol (1.0 mL) was then added to the obtained mixture. The resulting mixture was stirred at room temperature for 30 minutes. The reaction mixture was loaded onto a Varian™ SCX column and washed with methanol (16 mL). The obtained crude product was eluted with a 2 M methanol solution of NH3 (6 mL) and concentrated to thereby provide 1-(4-chlorobenzyl)-4-[[N-(3,5-bis(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine (Compd. No. 1213) (24.0 mg, 90%). The purity was determined by RPLC/MS (100%). ESI/MS m/e 536.2 (M++H, C24H24ClF6N3O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390830B1
출처 데이터셋uspto-grants-2008_06
ORD IDord-8a61569f96114cb8bb403549dc6d81ad
출처 메모uspto-grants-2008_06