Hydrochloric Acid → 6-(Piperidin-4-ylidenemethyl)-1,3-dihydroindol-2-one

HRID 1295585ノート

反応式

HRID 1295585 の反応式
C(OC([N:8]1[CH2:13][CH2:12][C:11](=[CH:14][C:15]2[CH:20]=[CH:19][C:18]([CH:21](C(OC)=O)[C:22](OC)=[O:23])=[C:17]([N+:30]([O-])=O)[CH:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[Sn].Cl>C(O)C>[NH:8]1[CH2:13][CH2:12][C:11](=[CH:14][C:15]2[CH:16]=[C:17]3[C:18]([CH2:21][C:22](=[O:23])[NH:30]3)=[CH:19][CH:20]=2)[CH2:10][CH2:9]1

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 5352426Tin atomHCID 86597572Dimethyl 2-[4-(1-tert-butoxycarbonylpiperidin-4-ylidenemethyl)-2-nitrophenyl]malonate

生成物 1

HCID 179651476-(Piperidin-4-ylidenemethyl)-1,3-dihydroindol-2-one収率 81%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Dimethyl 2-[4-(1-tert-butoxycarbonylpiperidin-4-ylidenemethyl)-2-nitrophenyl]malonate (1.65 g; 3.7 mmol) was dissolved in ethanol (50 ml), tin powder (1.31 g; 11 g atom) was added followed by conc. hydrochloric acid (10 ml) and the mixture heated at reflux for 3 h before being left to stand at ambient temperature for 18 h. Evaporated to dryness under reduced pressure, water added to the residue and the insoluble material removed by filtration. The filtrate and washings were combined and evaporated to dryness under reduced pressure and this residue extracted with hot methanol. The insoluble materials were further extracted with hot ethanol, the extracts combined and evaporated to dryness under reduced pressure to give the title compound (680 mg; 81%) as a brown foam.

後処理

  1. temperaturethe mixture heated
  2. temperatureat reflux for 3 h
  3. waitbefore being left
  4. customEvaporated to dryness under reduced pressure, water
  5. additionadded to the residue
  6. customthe insoluble material removed by filtration
  7. customevaporated to dryness under reduced pressure
  8. extractionthis residue extracted with hot methanol
  9. extractionThe insoluble materials were further extracted with hot ethanol
  10. customevaporated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-3a3d40da95814a258da6edf390484da5
出典データセット
uspto-grants-2007_07
特許番号
US07244726B2

反応ノート

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