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

HRID 1468956
ノート
印刷プレビュー

反応式

HRID 1468956 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
60 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-78001c445ed240a092fbfd6b97219fc8
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09006250B2

反応ノート

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