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Hydrochloric Acid → HCID 178526697、化合物

HRID 1261227
ノート
印刷プレビュー

反応式

HRID 1261227 の反応式
[F:1][C:2]1[CH:30]=[C:29]([N+:31]([O-:33])=[O:32])[CH:28]=[CH:27][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][N:8]=[C:7]2[CH:11]=[C:12]([C:14]3[N:15]=[CH:16][N:17](COCC[Si](C)(C)C)[CH:18]=3)[S:13][C:6]=12.Cl>CCO>[F:1][C:2]1[CH:30]=[C:29]([N+:31]([O-:33])=[O:32])[CH:28]=[CH:27][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][N:8]=[C:7]2[CH:11]=[C:12]([C:14]3[N:15]=[CH:16][NH:17][CH:18]=3)[S:13][C:6]=12
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

4

反応物 2

HCID 313Hydrochloric AcidHCID 594245697-(2-Fluoro-4-nitrophenoxy)-2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)thieno[3,2-b]pyridine

生成物 1

HCID 178526697HCID 178526697、化合物収率 100%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
85 °C

実験手順

To a suspension of 92 (3.3 g, 6.8 mmol) in EtOH (8 ml) was added concentrated HCl (7 ml) and distilled water (4 ml). The mixture was heated at 80-90° C. for 2.5 h, cooled to room temperature and concentrated under reduced pressure. The remaining residue was subjected to azeotropic distillation with EtOH followed by neutralization with saturated aqueous NaHCO3. The solid that precipitated was filtered and washed with water, and the filtrate was extracted with EtOAc. The solid and EtOAc extract were combined, evaporated under reduced pressure and the residue was collected and dried to afford the title compound 93 (2.4 g, 100% yield) as a yellow solid. MS (m/z) 357.0 (M+H).

後処理

  1. distillationdistilled water (4 ml)
  2. temperaturecooled to room temperature
  3. concentrationconcentrated under reduced pressure
  4. distillationThe remaining residue was subjected to azeotropic distillation with EtOH
  5. customThe solid that precipitated
  6. filtrationwas filtered
  7. washwashed with water
  8. extractionthe filtrate was extracted with EtOAc
  9. extractionThe solid and EtOAc extract
  10. customevaporated under reduced pressure
  11. customthe residue was collected
  12. customdried

出典と根拠

ORDレコード
ord-a75e6aea550443439fd554a147c1009e
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08470850B2

反応ノート

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