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HCID 68971803, 화합물 → HCID 69084677, 화합물

HRID 1992595
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HRID 1992595 반응식
[CH3:1][C:2]1[N:7]2[N:8]=[N:9][N:10]=[C:6]2[C:5]([N+:11]([O-])=O)=[C:4]([NH:14][CH2:15][CH2:16][CH2:17][OH:18])[C:3]=1[CH3:19]>[Pd].C(#N)C>[NH2:11][C:5]1[C:6]2[N:7]([N:8]=[N:9][N:10]=2)[C:2]([CH3:1])=[C:3]([CH3:19])[C:4]=1[NH:14][CH2:15][CH2:16][CH2:17][OH:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68971803HCID 68971803, 화합물

생성물 1

HCID 69084677HCID 69084677, 화합물수율 98.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 6342Acetonitrile용매

실험 절차

A mixture of 3-[(5,6-dimethyl-8-nitrotetraazolo[1,5-α]pyridin-7-yl)amino]propan-1-ol (4.00 g, 15.0 mmol) and 10% palladium on carbon (0.40 g) in acetonitrile (75 mL) was hydrogenated at 50 psi (3.5×105 Pa) on a Parr apparatus for 16 hours. The mixture was filtered through CELITE filter agent, which was rinsed with methanol. The filtrate was concentrated under reduced pressure to yield 3.48 g of 3-[(8-amino-5,6-dimethyltetraazolo[1,5-α]pyridin-7-yl)amino]propan-1-ol.

후처리

  1. filtrationThe mixture was filtered through CELITE
  2. filtrationfilter agent, which
  3. washwas rinsed with methanol
  4. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-881f04af0a6c4b82951848056586ada7
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07648997B2

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