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Iodine → Methyl 4-amino-3,6-dichloro-5-iodopicolinate

HRID 1468956
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HRID 1468956 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([C:9]([O:11][CH3:12])=[O:10])[C:3]=1[Cl:13].[I:14](O)(=O)(=O)=O.II>CO>[NH2:1][C:2]1[C:7]([I:14])=[C:6]([Cl:8])[N:5]=[C:4]([C:9]([O:11][CH3:12])=[O:10])[C:3]=1[Cl:13]
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참가 물질

5

반응물 3

HCID 807IodineHCID 65185Metaperiodic acidHCID 22677331Methyl 4-amino-3,6-dichloropyridine-2-carboxylate

생성물 1

HCID 90403719Methyl 4-amino-3,6-dichloro-5-iodopicolinate수율 208.7%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
60 °C

실험 절차

Methyl 4-amino-3,6-dichloropicolinate (10.0 g, 45.2 millimoles (mmol)), periodic acid (3.93 g, 17.2 mmol), and iodine (11.44 g, 45.1 mmol) were dissolved in methanol (30 mL) and refluxed at 60° C. for 27 h. The reaction mixture was concentrated, diluted with diethyl ether, and washed twice with saturated aqueous sodium bisulfite. The aqueous layers were extracted once with diethyl ether, and the combined organic layers were dried over anhydrous sodium sulfate. The product was concentrated and purified by flash chromatography (silica gel, 0-50% ethyl acetate/hexanes) to provide the title compound as a pale yellow solid (12.44 g, 35.9 mmol, 79%): mp 130.0-131.5° C.; 1H NMR (400 MHz, CDCl3) δ 5.56 (s, 2H), 3.97 (s, 3H); 13C NMR (101 MHz, CDCl3) δ 163.80, 153.00, 152.75, 145.63, 112.12, 83.91, 53.21; EIMS m/z 346.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with diethyl ether
  3. washwashed twice with saturated aqueous sodium bisulfite
  4. extractionThe aqueous layers were extracted once with diethyl ether
  5. dry with materialthe combined organic layers were dried over anhydrous sodium sulfate
  6. concentrationThe product was concentrated
  7. custompurified by flash chromatography (silica gel, 0-50% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-78001c445ed240a092fbfd6b97219fc8
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006250B2

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