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Toluene → Methyl 3-amino-6-chloropicolinate

HRID 887728
ノート
印刷プレビュー

反応式

HRID 887728 の反応式
[NH2:1][C:2]1[C:3]([C:9]([OH:11])=[O:10])=[N:4][C:5]([Cl:8])=[CH:6][CH:7]=1.[C:12]1(C)C=CC=CC=1.C[Si](C=[N+]=[N-])(C)C>CO>[CH3:12][O:10][C:9]([C:3]1[C:2]([NH2:1])=[CH:7][CH:6]=[C:5]([Cl:8])[N:4]=1)=[O:11]
参加物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 1140TolueneHCID 167693Trimethylsilyldiazomethane2 回HCID 533934343-Amino-6-chloropyridine-2-carboxylic acid

生成物 1

HCID 58964429Methyl 3-amino-6-chloropicolinate

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

3-Amino-6-chloro-pyridine-2-carboxylic acid (636 mg) was suspended in methanol (8 mL) and toluene (22 mL) was added. A solution of (trimethylsilyl)diazomethane (2.0 M in hexane, 2.4 mL) was added slowly to the reaction mixture. After 1 hour stirring at room temperature, another portion of (trimethylsilyl)diazomethane (550 μl) was added and the mixture was stirred for additional 45 minutes. The reaction mixture was quenched with water and extracted 3× with ethyl acetate. The combined organic layer was washed with 2N hydrochloric acid, saturated bicarbonate solution and brine, dried over MgSO4 and concentrated in vacuum. The residue was purified by column chromatography (silica gel 60, choroform/ethyl acetate=50:1, Rf=0.30) to afford 365 mg of the title compound of the formula

後処理

  1. stirringthe mixture was stirred for additional 45 minutes
  2. customThe reaction mixture was quenched with water
  3. extractionextracted 3× with ethyl acetate
  4. washThe combined organic layer was washed with 2N hydrochloric acid, saturated bicarbonate solution and brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuum
  7. customThe residue was purified by column chromatography (silica gel 60, choroform/ethyl acetate=50:1, Rf=0.30)

出典と根拠

ORDレコード
ord-8a6a8d0b438c4ed88cbd54e7832eb103
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08247431B2

反応ノート

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