홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

1'-Benzyl-5H-spiro[furo[3,4-b]pyridine-7,4'-piperidine] → 5H-Spiro[furo[3,4-b]pyridine-7,4'-piperidine]

HRID 1663337
노트
인쇄 미리보기

반응식

HRID 1663337 반응식
C([N:8]1[CH2:13][CH2:12][C:11]2([C:17]3=[N:18][CH:19]=[CH:20][CH:21]=[C:16]3[CH2:15][O:14]2)[CH2:10][CH2:9]1)C1C=CC=CC=1>C(O)C.[Pd]>[NH:8]1[CH2:9][CH2:10][C:11]2([C:17]3=[N:18][CH:19]=[CH:20][CH:21]=[C:16]3[CH2:15][O:14]2)[CH2:12][CH2:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 597568191'-Benzyl-5H-spiro[furo[3,4-b]pyridine-7,4'-piperidine]

생성물 1

HCID 597568245H-Spiro[furo[3,4-b]pyridine-7,4'-piperidine]수율 91%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of 0.39 g (1.4 mmol) 1′-benzyl-5H-spiro[furo[3,4-b]pyridine-7,4′-piperidine] in 14 ml ethanol was purged with argon prior to adding 0.15 g (10 mol %) palladium on activated charcoal. The flask was evacuated, refilled with hydrogen gas and stirred at room temperature under an atmosphere of hydrogen for 16 h. The catalyst was filtered off and washed with ethanol. The filtrate was concentrated to dryness to give the title compound (0.24 g, 91%) as an amorphous solid.

후처리

  1. customThe flask was evacuated
  2. additionrefilled with hydrogen gas
  3. filtrationThe catalyst was filtered off
  4. washwashed with ethanol
  5. concentrationThe filtrate was concentrated to dryness

출처 및 근거

ORD 기록
ord-ebcabceb1ccd42958554a98d213b2cfc
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08034937B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트