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Triphenylphosphine → 4-{2-[4-(3,6-Dichloro-pyridazin-4-yl)-piperazin-1-yl]ethoxy}-phenylacetic acid methyl ester

HRID 657598
ノート
印刷プレビュー

反応式

HRID 657598 の反応式
[Cl:1][C:2]1[N:3]=[N:4][C:5]([Cl:17])=[CH:6][C:7]=1[N:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][OH:16])[CH2:10][CH2:9]1.[CH2:18]([O:20][C:21](=[O:29])[C:22]1[CH:27]=[CH:26][C:25](O)=NC=1)C.[C:30]1(P(C2C=CC=CC=2)C2C=CC=CC=2)[CH:35]=CC=C[CH:31]=1.N(C(OCC)=O)=NC(OCC)=O>O1CCCC1>[CH3:18][O:20][C:21](=[O:29])[CH2:22][C:27]1[CH:26]=[CH:25][C:35]([O:16][CH2:15][CH2:14][N:11]2[CH2:10][CH2:9][N:8]([C:7]3[CH:6]=[C:5]([Cl:17])[N:4]=[N:3][C:2]=3[Cl:1])[CH2:13][CH2:12]2)=[CH:30][CH:31]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 817655582-[4-(3,6-Dichloropyridazin-4-yl)-piperazin-1-yl]-ethanolHCID 178469094HCID 178469094、化合物

生成物 1

HCID 159847264-{2-[4-(3,6-Dichloro-pyridazin-4-yl)-piperazin-1-yl]ethoxy}-phenylacetic acid methyl ester収率 42.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a 50 mL dry three-necked flask, 0.554 g (0.002 mol) of self-made 2-[4-(3,6-dichloro-pyridazin-4-yl)-piperazin-1-yl]-ethanol, 0.28 g (0.002 mol) of 6-hydroxy-nicotinic acid ethyl ester, 0.612 g of triphenylphosphine were added, 15 mL of anhydrous tetrahydrofuran was poured into the flask under condition of ice bath and nitrogen gas protection, then 0.35 mL of diethyl azodiformate (DEAD) dissolved in 5 mL of anhydrous tetrahydrofuran was added dropwise into the flask, after the dropwise addition, the temperature was elevated to room temperature, the agitation was kept overnight. The solvent was removed by evaporation using a rotation evaporator next day, the residue was poured into 100 mL of water, extracted for three times using total 150 mL of dichloromethane, the extract solutions were combined together, dried over anhydrous Na2SO4, concentrated, and separated by column chromatograph (eluent, petroleum ether:ethyl acetate:methanol=10:5:0.15) to obtain 0.32 g of 4-{2-[4-(3,6-dichloro-pyridazin-4-yl)-piperazin-1-yl]-ethoxy}-phenylacetic acid methyl ester, a white solid. Yield: 42.3%, m.p. 140˜141° C. 1H-NMR (400MHz, CDCl3) δppm: 1.37˜1.41(t, 3H, J=7.3Hz), 2.79(brs, 4H), 2.91(brs, 2H), 3.36(brs, 4H), 4.35˜4.40(q, 2H, J=7.3Hz), 4.57(brs, 2H), 6.78˜6.80(d, 2H, J=8.7Hz), 6.86(s, 1H), 8.16˜8.18(dd, 1H, J1=8.7Hz, J2=2.2Hz).

後処理

  1. additionwas added dropwise into the flask
  2. additionafter the dropwise addition
  3. customwas elevated to room temperature
  4. customThe solvent was removed by evaporation
  5. customa rotation evaporator next day
  6. additionthe residue was poured into 100 mL of water
  7. extractionextracted for three times
  8. dry with materialdried over anhydrous Na2SO4
  9. concentrationconcentrated
  10. customseparated by column chromatograph (eluent, petroleum ether:ethyl acetate:methanol=10:5:0.15)

出典と根拠

ORDレコード
ord-ef959f9924ff426ea4b97acd917da8b3
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08076339B2

反応ノート

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