Sulfuric Acid → 1-Benzhydryl-3-ethylaminoazetidine-3-carboxylic Acid Amide

HRID 1246797ノート

反応式

HRID 1246797 の反応式
[CH:1]([N:14]1[CH2:17][C:16]([NH:20][CH2:21][CH3:22])([C:18]#[N:19])[CH2:15]1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:23]S(O)(=O)=O>C(Cl)Cl.C(OCC)(=O)C>[CH:1]([N:14]1[CH2:17][C:16]([NH:20][CH2:21][CH3:22])([C:18]([NH2:19])=[O:23])[CH2:15]1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

5

反応物 2

HCID 1118Sulfuric AcidHCID 219058181-Benzhydryl-3-ethylaminoazetidine-3-carbonitrile

生成物 1

HCID 587217631-Benzhydryl-3-ethylaminoazetidine-3-carboxylic Acid Amide

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A vigorously stirred solution of 1-benzhydryl-3-ethylaminoazetidine-3-carbonitrile (I-(13A-9)d; 11.7 g, 40 mmol) in methylene chloride (150 ml) cooled in an ice bath was treated with H2SO4 (22 ml, 0.4 mol), dropwise. After the reaction mixture was allowed to warm to room temperature and stir overnight, it was cooled in an ice bath and then carefully quenched with concentrated NH4OH to pH 11. The off-white solids that formed during the quench were collected by vacuum filtration. The aqueous mixture was then extracted with methylene chloride, the combined organic layers were washed with brine, dried (Na2SO4) and then concentrated, in vacuo, to afford additional solids. The combined solids were stirred for 1 hour in ethyl acetate (150 mL) and then collected by vacuum filtration to give I-(13A-9)e (9.2 g, 74%) as a solid: +ES MS (M+1) 310.2; 1H NMR (400 MHz, CD3OD) δ 7.41 (d, J=7.1 Hz, 4H), 7.25 (t, J=7.5 Hz, 4H), 7.16 (t, J=7.5 Hz, 2H), 4.49 (s, 1H), 3.44 (d, J=8.3 Hz, 2H), 3.11 (d, J=8.3 Hz, 2H), 2.47 (q, J=7.1 Hz, 2H), 1.10 (t, J=7.3 Hz, 3H).

後処理

  1. temperatureit was cooled in an ice bath
  2. customcarefully quenched with concentrated NH4OH to pH 11
  3. customThe off-white solids that formed during the quench
  4. filtrationwere collected by vacuum filtration
  5. extractionThe aqueous mixture was then extracted with methylene chloride
  6. washthe combined organic layers were washed with brine
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated, in vacuo
  9. customto afford additional solids
  10. filtrationcollected by vacuum filtration
  11. customto give I-(13A-9)e (9.2 g, 74%) as a solid

出典と根拠

ORDレコード
ord-43711c43830d4b90a2cb292719c4a29b
出典データセット
uspto-grants-2006_10
特許番号
US07129239B2

反応ノート

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