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Hydrochloric Acid → HCID 90047521、化合物

HRID 1507601
ノート
印刷プレビュー

反応式

HRID 1507601 の反応式
C([NH:8][C:9]1[N:14]=[C:13]2[N:15]([CH3:21])[C:16](=[O:20])[C:17]([CH3:19])([CH3:18])[C:12]2=[CH:11][CH:10]=1)C1C=CC=CC=1.[ClH:22]>C(O)C.[Pd]>[ClH:22].[NH2:8][C:9]1[N:14]=[C:13]2[N:15]([CH3:21])[C:16](=[O:20])[C:17]([CH3:18])([CH3:19])[C:12]2=[CH:11][CH:10]=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

5

反応物 2

HCID 313Hydrochloric AcidHCID 90047615HCID 90047615、化合物

生成物 1

HCID 90047521HCID 90047521、化合物

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

反応条件

温度
40 °C

実験手順

A mixture of 6-(benzylamino)-1,3,3-trimethyl-1H-pyrrolo[2,3-b]pyridin-2(3H)-one (610 mg, 2.17 mmol) and 25% aqueous HCl solution (1.2 g, 1 ml, 8.23 mmol) in ethanol (20 ml) was evacuated three times and flushed with argon. Pd (10% on activated charcoal, 231 mg, 217 μmol) was added. Degassing was repeated, then evacuated three times and flushed with hydrogen. The reaction mixture was heated to 40° C. and stirred 4 hours at this temperature under the hydrogen atmosphere. The reaction mixture was filtered through a glass fiber filter, washed with EtOH and the solvent was evaporated. The title compound was obtained as grey solid (388 mg) and was used without further purification.

後処理

  1. customwas evacuated three times
  2. customflushed with argon
  3. customDegassing
  4. customevacuated three times
  5. customflushed with hydrogen
  6. filtrationThe reaction mixture was filtered through a glass fiber
  7. filtrationfilter
  8. washwashed with EtOH
  9. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-76f5e7124ad44ec9a6e9b92632b1cbd6
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09221816B2

反応ノート

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