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5-Chloro-4-methyl-3-nitropyridin-2-amine → HCID 68532432, 화합물

HRID 2374164
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HRID 2374164 반응식
[Cl:1][C:2]1[C:3]([CH3:12])=[C:4]([N+:9]([O-])=O)[C:5]([NH2:8])=[N:6][CH:7]=1.[H][H]>CO.O=[Pt]=O>[ClH:1].[Cl:1][C:2]1[C:3]([CH3:12])=[C:4]([NH2:9])[C:5]([NH2:8])=[N:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 214641365-Chloro-4-methyl-3-nitropyridin-2-amineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 68532432HCID 68532432, 화합물수율 193.3%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 887Methanol용매

실험 절차

The material from Step 1 (1.0 g) was dissolved in MeOH (300 ml) and PtO2 (40 mg) was added. The mixture was subjected to hydrogen (50 psi) in a Parr shaker for 3.5 h, then filtered through Celite and to the filtrate was added conc. HCl (1 ml) before concentrating to yield 5-chloro-4-methyl-pyridine-2,3-diamine hydrochloride (1 g). NMR (CDCl3) δ 7.39 (s, 1H), 2.29 (s, 3H).

후처리

  1. filtrationfiltered through Celite and to the filtrate
  2. additionwas added conc. HCl (1 ml)
  3. concentrationbefore concentrating

출처 및 근거

ORD 기록
ord-1b9cd93415cc458a8d7ce382b2a97452
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07462600B2

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