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1-[3-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]-3-pyrrolidinecarbonitrile → 1-(3-Aminopropyl)-3-pyrrolidinecarbonitrile

HRID 1669214
ノート
印刷プレビュー

反応式

HRID 1669214 の反応式
O=C1C2C(=CC=CC=2)C(=O)[N:3]1[CH2:12][CH2:13][CH2:14][N:15]1[CH2:19][CH2:18][CH:17]([C:20]#[N:21])[CH2:16]1>CCO>[NH2:3][CH2:12][CH2:13][CH2:14][N:15]1[CH2:19][CH2:18][CH:17]([C:20]#[N:21])[CH2:16]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

3

反応物 1

HCID 577865711-[3-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]-3-pyrrolidinecarbonitrile

生成物 1

HCID 574476861-(3-Aminopropyl)-3-pyrrolidinecarbonitrile

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
5 °C

実験手順

A solution of phthalimide 303 (5.96 g, 21.0 mmol) and N2H4.H2O (2.04 mL, 42.0 mmol in EtOH (60 mL) was stirred at reflux temperature for 2 h. The solution was cooled to 5° C. for 2 h, the precipitate filtered, washed with EtOH (5 mL) and the filtrate evaporated to half volume. The solution was cooled at 5° C. for a further 2 h, the precipitate filtered, washed with EtOH (5 mL) and the filtrate evaporated to give diamine 304 which was used without further purification: 1H NMR δ 2.94-3.02 (m, 1H, CHCN), 2.90 (dd, J=9.0, 7.9 Hz, 1H, CH2), 2.82 (t, J=6.8 Hz, 2H, CH2N), 2.61-2.68 (m, 2H, CH2N), 2.48-2.58 (m, 3H, CH2N), 2.05-2.15 (m, 1H, CH2), 2.03-2.11 (m, 1H, CH2), 1.68 (p, J=7.0 Hz, 2H, CH2), NH2 not observed.

後処理

  1. temperatureat reflux temperature for 2 h
  2. filtrationthe precipitate filtered
  3. washwashed with EtOH (5 mL)
  4. customthe filtrate evaporated to half volume
  5. temperatureThe solution was cooled at 5° C. for a further 2 h
  6. filtrationthe precipitate filtered
  7. washwashed with EtOH (5 mL)
  8. customthe filtrate evaporated

出典と根拠

ORDレコード
ord-55088f1bdcd643038721cd76ce15dcd7
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989451B2

反応ノート

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