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HCID 86608958、化合物 → HCID 68408133、化合物

HRID 1710811
ノート
印刷プレビュー

反応式

HRID 1710811 の反応式
[CH3:1][Li].[NH2:3][C:4]1[C:15]([Cl:16])=[CH:14][CH:13]=[C:12]([Cl:17])[C:5]=1[C:6](N(OC)C)=[O:7]>O1CCCC1.O>[NH2:3][C:4]1[C:15]([Cl:16])=[CH:14][CH:13]=[C:12]([Cl:17])[C:5]=1[C:6](=[O:7])[CH3:1]
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 2

HCID 86608958HCID 86608958、化合物HCID 178418348HCID 178418348、化合物

生成物 1

HCID 68408133HCID 68408133、化合物収率 29%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

At −78° C. a solution of methyl lithium (1.6M in diethyl ether, 25 ml, 40 mmol) was added dropwise to a solution of 2-amino-3,6-dichloro-N-methoxy-N-methyl-benzamide (2.5 g, 10 mmol) in tetrahydrofurane (100 ml). After complete addition, the reaction was warmed to r.t. The dark solution was stirred for 3 hours at room temperature. Under ice cooling 2N aqueous hydrochloride solution (25 ml) was added dropwise and stirred at r.t. for 30 minutes. The reaction was diluted with water, extracted twice with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and the solvent was evaporated. The residue was purified by column chromatography (silica gel, solvent gradient n-heptan/ethyl acetate=3/7) to yield the title compound as an orange oil (0.59 g, 29%).

後処理

  1. additionAfter complete addition
  2. additionUnder ice cooling 2N aqueous hydrochloride solution (25 ml) was added dropwise
  3. stirringstirred at r.t. for 30 minutes
  4. extractionextracted twice with ethyl acetate
  5. washThe combined organic layers were washed with saturated aqueous sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customthe solvent was evaporated
  9. customThe residue was purified by column chromatography (silica gel, solvent gradient n-heptan/ethyl acetate=3/7)

出典と根拠

ORDレコード
ord-04206ae683d9403aacbe3e3ad6ad66bf
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07790732B2

反応ノート

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