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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 525459생성일: 2026년 10월 26일

4-Piperidineacetic acid → HCID 60162961, 화합물

https://huagongshe.com/reaction/525459

반응식

참여 물질

역할이름HCID투입량
반응물4-Piperidineacetic acidHCID 1512594—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-4-ethyl-piperidine-4-carboxylic acidHCID 60162828—
반응물6-(trans-4-Tert-butylcyclohexyloxy)-2-naphthaldehydeHCID 86668412—
생성물HCID 60162961HCID 6016296160%

반응 단계

The compound was prepared in a manner similar as to that described for 1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-4-ethyl-piperidine-4-carboxylic acid using Piperidin-4-yl-acetic acid (0.0554 g, 0.387 mmol), 6-(4-tert-Butyl-cyclohexyloxy)-naphthalene-2-carbaldehyde (0.100 g, 0.322 mmol) and Sodium triacetoxyborohydride (0.212 g, 0.9 mol) to give 85 mg {1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-piperidin-4-yl}-acetic acid (60%). ESI-LCMS (438 M+H). 1H NMR (DMSO-d6, 400 MHz): Shift (ppm) 7.71-8.01 (m, 3H), 7.43 (d, J=2.0 Hz, 2H), 7.10-7.30 (m, 1H), 4.38 (d, J=4.8 Hz, 3H), 3.28-3.55 (m, 2H), 2.82-3.14 (m, 2H), 2.20 (d, J=6.3 Hz, 4H), 1.85 (br. s., 5H), 1.38 (br. s., 7H), 0.89 (s, 9H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340527B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-a914696fb58b4be9980dfab23fa814b7
출처 메모uspto-grants-2016_05