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HRID 1361517생성일: 2026년 10월 26일

4-(5-Chloro-2-methoxy-phenyl)-4-methoxy-piperidine-1-carboxylic acid tert-butyl ester → Hydrochloric Acid

https://huagongshe.com/reaction/1361517

반응식

참여 물질

역할이름HCID투입량
반응물4-(5-Chloro-2-methoxy-phenyl)-4-methoxy-piperidine-1-carboxylic acid tert-butyl esterHCID 58772528—
용매Hydrochloride methanolHCID 21893726—
생성물Hydrochloric AcidHCID 313—
생성물4-(5-Chloro-2-methoxyphenyl)-4-methoxypiperidineHCID 58772297—

반응 단계

A solution of 4-(5-chloro-2-methoxy-phenyl)-4-methoxy-piperidine-1-carboxylic acid tert-butyl ester 5c (3.8 g, crude from last step) in methanol/HCl (2 M, 50 mL) was stirred at room temperature for 4 h, then the mixture was concentrated to half of volume under 40° C. and then ether was added. The precipitated was filtered and washed with ether to obtain 4-(5-chloro-2-methoxyphenyl)-4-methoxypiperidine 5d as its HCl salt. 1H NMR (DMSO-d6): δ 8.95 (b, 2H), 7.37-7.34 (q, J1=8.8 Hz, J2=8.8 Hz, 1H), 7.21-7.20 (d, J=2.8 Hz, 1H), 7.09-7.07 (d, J=8.8 Hz, 1H), 3.78 (s, 3H), 3.16-3.13 (m, 2H), 3.13-2.98 (m, 5H), 2.35-2.28 (m, 2H), 2.19-2.16 (m, 2H). ESI-MS m/z 256.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07880007B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-38d2ce59f83649bfb3dad518bd2060c6
출처 메모uspto-grants-2011_02