Dimethylformamide → ethyl N-(4-[(4-pyridyl)piperazin-1-yl]benzoyl)-N-methylglycinate

HRID 1291888

反応式

HRID 1291888 の反応式
[N:1]1[CH:6]=[CH:5][C:4]([CH:7]2[CH2:12][NH:11][CH2:10][CH2:9][N:8]2[C:13]2[CH:21]=[CH:20][C:16](C(O)=O)=[CH:15][CH:14]=2)=[CH:3][CH:2]=1.C1C=CC2N([OH:31])N=NC=2C=1.CN([C:35]([O:39]N1N=NC2C=CC=CC1=2)=[N+:36]([CH3:38])[CH3:37])C.F[P-](F)(F)(F)(F)F.C(N([CH:62]([CH3:64])C)CC)(C)C.CN([CH:68]=[O:69])C>O>[N:1]1[CH:2]=[CH:3][C:4]([CH:7]2[CH2:12][NH:11][CH2:10][CH2:9][N:8]2[C:13]2[CH:21]=[CH:20][C:16]([C:35]([N:36]([CH3:37])[CH2:38][C:68]([O:69][CH2:62][CH3:64])=[O:31])=[O:39])=[CH:15][CH:14]=2)=[CH:5][CH:6]=1

参加物

7

反応物 5

HCID 6228DimethylformamideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 189183004-((4-Pyridyl)piperazin-1-yl)benzoic acid

生成物 1

HCID 18918248ethyl N-(4-[(4-pyridyl)piperazin-1-yl]benzoyl)-N-methylglycinate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a stirred mixture of 4-[(4-pyridyl)piperazin-1-yl]benzoic acid (prepared as in Example 56(i)) (311 mg), HOBt.H2O (170 mg) and HBTU (416 mg) in DMF (5 ml) at 0°-5° C. under argon was added diisopropylethylamine (0.75 ml). The ice-bath was removed and the reaction mixture was stirred at room temperature for 15 minutes before solid sarcosine, ethyl ester hydrochloride (154 mg) was added. The reaction mixture was stirred at room temperature under argon overnight then diluted with dichloromethane (30 ml) and water (30 ml). The organic layer was separated and the aqueous layer was re-extracted with dichloromethane (30 ml). The combined organic extracts were washed with water, saturated sodium bicarbonate solution, water, dried (MgSO4) and evaporated. The residue was purified by filtration through a short bed of activated (grade II) alumina by elution with ethyl acetate/methanol, 5:1, to give ethyl N-(4-[(4-pyridyl)piperazin-1-yl]benzoyl)-N-methylglycinate (92 mg) as an amorphous solid: NMR (d6 -DMSO+CD3CO2D) δ 1.18 (3H, t), 2.98 (3H, s), 3.44 (4H, m), 3.79 (4H, m), 4.11 (4H, m), 6.94 (2H, d), 7.12 (2H, d), 7.31 (2H, br, d), 8.19 (2H, d); m/Z 383 (M+H)+.

後処理

  1. customThe ice-bath was removed
  2. additionwas added
  3. stirringThe reaction mixture was stirred at room temperature under argon overnight
  4. additionthen diluted with dichloromethane (30 ml) and water (30 ml)
  5. customThe organic layer was separated
  6. extractionthe aqueous layer was re-extracted with dichloromethane (30 ml)
  7. washThe combined organic extracts were washed with water, saturated sodium bicarbonate solution, water
  8. dry with materialdried (MgSO4)
  9. customevaporated
  10. filtrationThe residue was purified by filtration through a short bed of activated (grade II) alumina by elution with ethyl acetate/methanol, 5:1

出典と根拠

ORDレコード
ord-92e044bf43de40678c94c751a0a7b616
出典データセット
uspto-grants-1998_05
特許番号
US05753659

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