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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-[6-(Azidomethyl)-2-pyridyl]propan-2-ol → 2-(6-(Aminomethyl)pyridin-2-yl)propan-2-ol

HRID 2096678
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HRID 2096678 반응식
[N:1]([CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([OH:14])([CH3:13])[CH3:12])[N:6]=1)=[N+]=[N-]>CO.[Pd]>[OH:14][C:11]([C:7]1[N:6]=[C:5]([CH2:4][NH2:1])[CH:10]=[CH:9][CH:8]=1)([CH3:13])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 866553202-[6-(Azidomethyl)-2-pyridyl]propan-2-ol

생성물 1

HCID 667184282-(6-(Aminomethyl)pyridin-2-yl)propan-2-ol수율 90.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

2-Azidomethyl-6-(1-hydroxy-1-methylethyl)pyridine (5.88 g, 30.6 mmol) was dissolved in methanol (100 mL) and palladium (5% w/w on carbon) added. The suspension was gently agitated under a hydrogen atmosphere overnight, filtered though celite and concentrated to dryness to give 4.61 g (90%) of the amine as a colorless oil; NMR δH (400 MHz, CDCl3) 7.63 (1H, t, J 7.8 Hz), 7.19 (1H, d, J 7.8 Hz), 7.12 (1H, d, J 7.6 Hz), 3.93 (2H, s), 1.49 (6H, s); LC-MS Retention time 0.42 min, (M+H)+ 167.

후처리

  1. filtrationfiltered though celite and
  2. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-d95f7796589d4683be3b888dd6f46e49
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450328B2

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