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Sodium Hydroxide → (2,6-difluorophenyl)-N-[5-(7-methyl-2H,3H-benzo[e]1,4-dioxin-6-yl)(2-pyridyl)]carboxamide

HRID 874668
ノート
印刷プレビュー

反応式

HRID 874668 の反応式
[CH3:1][C:2]1[C:3]([C:12]2[CH:13]=[CH:14][C:15]([NH2:18])=[N:16][CH:17]=2)=[CH:4][C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[CH:11]=1.[Cl-].[F:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[CH:22]=1.[CH:28](N(C(C)C)CC)(C)C.[OH-:37].[Na+]>C(Cl)Cl.CN(C)C1C=CN=CC=1>[F:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:22]=1[C:28]([NH:18][C:15]1[CH:14]=[CH:13][C:12]([C:3]2[C:2]([CH3:1])=[CH:11][C:6]3[O:7][CH2:8][CH2:9][O:10][C:5]=3[CH:4]=2)=[CH:17][N:16]=1)=[O:37]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 14798Sodium HydroxideHCID 81531DiisopropylethylamineHCID 584873735-(7-methyl-2H,3H-benzo[e]1,4-dioxin-6-yl)-2-pyridylamineHCID 1317308842,6-Difluorobenzol chloride

生成物 1

HCID 58487156(2,6-difluorophenyl)-N-[5-(7-methyl-2H,3H-benzo[e]1,4-dioxin-6-yl)(2-pyridyl)]carboxamide収率 40%

試薬・触媒・溶媒 2

HCID 14284
4-(Dimethylamino)pyridine
触媒
HCID 6344Dichloromethane溶媒

実験手順

To a solution of 183 (30 mg, 0.12 mmol) in CH2Cl2 was added 4-dimethylaminopyridine (DMAP, 1.2 mg, 0.01 mmol), 2,6-difluorobenzol chloride (53 mg, 0.3 mmol) and diisopropylethylamine (DIEA, 62 mg, 0.48 mmol). The reaction mixture was stirred for 2 h at ambient temperature. The reaction was quenched with saturated NaHCO3 (20 ml) and extracted with EtOAc. The organic solvent was removed in vacuo. The residue was dissolved in THF:MeOH (1:1) and added 1N NaOH (2 eq). The mixture was stirred for 10 min at ambient temperature. The reaction solution was concentrated in vacuo and residue was extracted with EtOAc. The crude product was purified by ISCO column and HPLC. Fractions containing pure product were combined and evaporated. The white solid 185 (18.2 mg, 40%) was obtained. LC-MS: calcd. for C21H16F2N2O3: 383 (M+1).

後処理

  1. customThe reaction was quenched with saturated NaHCO3 (20 ml)
  2. extractionextracted with EtOAc
  3. customThe organic solvent was removed in vacuo
  4. dissolutionThe residue was dissolved in THF:MeOH (1:1)
  5. stirringThe mixture was stirred for 10 min at ambient temperature
  6. concentrationThe reaction solution was concentrated in vacuo and residue
  7. extractionwas extracted with EtOAc
  8. customThe crude product was purified by ISCO column and HPLC
  9. additionFractions containing pure product
  10. customevaporated

出典と根拠

ORDレコード
ord-c493d04bdf79453787cd663bab415146
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08980629B2

反応ノート

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