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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 525455생성일: 2026년 10월 26일

Acetic Acid → 1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-4-phenyl-piperidine-4-carboxylic acid

https://huagongshe.com/reaction/525455

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물MethanolHCID 887—
반응물4-Phenylpiperidine-4-carboxylic acid, compound with toluene-p-sulphonic acidHCID 19259—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-4-ethyl-piperidine-4-carboxylic acidHCID 60162828—
반응물6-(trans-4-Tert-butylcyclohexyloxy)-2-naphthaldehydeHCID 86668412—
생성물1-[6-(4-tert-Butyl-cyclohexyloxy)-naphthalen-2-ylmethyl]-4-phenyl-piperidine-4-carboxylic acidHCID 601628315%

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 4-Phenyl-piperidine-4-carboxylic acid (0.198 g, 0.967 mmol), 6-(4-tert-Butyl-cyclohexyloxy)-naphthalene-2-carbaldehyde (0.250 g, 0.805 mmol), acetic acid (0.16 mL, 2.8 mmol), Methanol (1.6 mL, 4.0E1 mmol) and sodium cyanoborohydride (75.314 mg, 1.1985 mmol) to give 21 mg of the title compound as a white solid (5%). ESI-LCMS (500 M+H). 1H NMR (DMSO-d6, 400 MHz): Shift (ppm) 7.80-7.98 (m, 3H), 7.16-7.63 (m, 8H), 4.51 (br. s., 3H), 3.45-3.64 (m, 2H), 2.96-3.18 (m, 2H), 2.68 (m, 2H), 2.13-2.31 (m, 2H), 1.74-2.09 (m, 4H), 1.00-1.53 (m, 5H), 0.89 (s, 9H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340527B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-bf3814db56784bd99ed0e081f31a535c
출처 메모uspto-grants-2016_05