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Toluene → Methyl 3-amino-6-chloropicolinate

HRID 887728
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HRID 887728 반응식
[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]
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참가 물질

5

반응물 3

HCID 1140TolueneHCID 167693Trimethylsilyldiazomethane2회HCID 533934343-Amino-6-chloropyridine-2-carboxylic acid

생성물 1

HCID 58964429Methyl 3-amino-6-chloropicolinate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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

후처리

  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)

출처 및 근거

ORD 기록
ord-8a6a8d0b438c4ed88cbd54e7832eb103
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08247431B2

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