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Methyl 4-fluorobenzoate → Methyl 4-(4-methyl-1,4-diazepan-1-yl)benzoate

HRID 16867
ノート
印刷プレビュー

反応式

HRID 16867 の反応式
[CH3:1][N:2]1[CH2:8][CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.F[C:10]1[CH:19]=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[CH:12][CH:11]=1>CC(N(C)C)=O>[CH3:1][N:2]1[CH2:8][CH2:7][CH2:6][N:5]([C:10]2[CH:19]=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[CH:12][CH:11]=2)[CH2:4][CH2:3]1
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

4

反応物 2

HCID 67878Methyl 4-fluorobenzoateHCID 2283491-Methylhomopiperazine

生成物 1

HCID 66589865Methyl 4-(4-methyl-1,4-diazepan-1-yl)benzoate収率 24.1%

試薬・触媒・溶媒 1

HCID 31374Dimethylacetamide溶媒

反応条件

温度
100 °C

実験手順

1-Methyl-1,4-diazepane (15.07 g, 132.00 mmol) was added to methyl 4-fluorobenzoate (7.76 mL, 60 mmol) in DMA (150 mL). The resulting solution was stirred at 100° C. for 40 h. The reaction mixture was evaporated and quenched with 2M sodium hydroxide (50 ml). This was extracted with DCM (3×50 ml). The combined organic extracts were washed with saturated brine (50 ml), dried over MgSO4, filtered and evaporated to dryness. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 10% MeOH in DCM. Pure fractions were evaporated to dryness to afford methyl 4-(4-methyl-1,4-diazepan-1-yl)benzoate (3.59 g, 24.10%) as a tan waxy solid.

後処理

  1. customThe reaction mixture was evaporated
  2. customquenched with 2M sodium hydroxide (50 ml)
  3. extractionThis was extracted with DCM (3×50 ml)
  4. washThe combined organic extracts were washed with saturated brine (50 ml)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated to dryness
  8. customThe crude product was purified by silica column chromatography
  9. washeluting with a gradient of 0 to 10% MeOH in DCM
  10. customPure fractions were evaporated to dryness

出典と根拠

ORDレコード
ord-71297f6e18f245419f536eb64c14b8be
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07737149B2

反応ノート

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