Ammonium formate → HCID 10464367、化合物

HRID 370364ノート

反応式

HRID 370364 の反応式
C([N:8]1[CH2:12][CH2:11][C@@H:10]([C@@H:13]([NH:15][CH3:16])[CH3:14])[CH2:9]1)C1C=CC=CC=1.C([O-])=O.[NH4+]>CO.[OH-].[OH-].[Pd+2].C(Cl)Cl.CO>[CH3:16][NH:15][C@H:13]([C@@H:10]1[CH2:11][CH2:12][NH:8][CH2:9]1)[CH3:14]

参加物

6

反応物 2

HCID 2723923Ammonium formateHCID 9904942HCID 9904942、化合物

生成物 1

HCID 10464367HCID 10464367、化合物

試薬・触媒・溶媒 3

HCID 9942167Palladium hydroxide触媒HCID 887Methanol溶媒HCID 21226129Dichloromethane methanol溶媒

実験手順

(R,S)-1-benzyl-3-[1'-(methylamino)ethyl]pyrrolidine (0.51 g of crude product) is dissolved in MeOH (10 ml) under a N2 atmosphere, Pearlman's catalyst and ammonium formate (0.89 g, 14.11 mmol) are then added. The reaction mixture is refluxed for 12 hours. The reaction mixture is then diluted with CH2Cl2 :MeOH (1:1) and filtered through a celite pad. The filtrate is washed with 15% aqueous NaOH:brine (1:1) and the aqueous layer is back extracted with CH2Cl2 (2×). The combined organic layers are dried over MgSO4, filtered and concentrated under a stream of N2 to give crude (R,S)-3-[1'-(methylamino)ethyl]pyrrolidine: 1H NMR (300 MHz, CDCl3) δ 1.05 (d, J is 6.3 Hz, 3H), 1.43 (ddd, J is 17, 12, 9 Hz, 1H), 1.87 (m, 1H), 2.02 (dd, J is 16, 8 Hz, 1H), 2.38 (s, 3H), 2.41 (m, 1H), 2.61 (broad s, 2H), 2.65 (dd, J is 11, 8 Hz, 1H), 2.91-3.00 (m, 2H), 3.13 (dd, J is 11, 8 Hz, 1H). This material is suitable for use in various reactions including but not limited to the synthesis of quinolones.

後処理

  1. temperatureThe reaction mixture is refluxed for 12 hours
  2. filtrationfiltered through a celite pad
  3. washThe filtrate is washed with 15% aqueous NaOH:brine (1:1)
  4. extractionthe aqueous layer is back extracted with CH2Cl2 (2×)
  5. dry with materialThe combined organic layers are dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under a stream of N2

出典と根拠

ORDレコード
ord-240182b5c2eb42ee87300d5b28f6cf85
出典データセット
uspto-grants-2000_10
特許番号
US06140510

反応ノート

読み込み中…