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Guanidine Hydrochloride → HCID 22260979、化合物

HRID 1610109
ノート
印刷プレビュー

反応式

HRID 1610109 の反応式
[Na].Cl.[NH2:3][C:4]([NH2:6])=[NH:5].CN(C)/[CH:9]=[CH:10]/[C:11]([C:13]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[NH:15][N:14]=1)=O.[Cl-].[NH4+]>C(O)C>[NH:15]1[C:16]2[C:21](=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:13]([C:11]2[CH:10]=[CH:9][N:3]=[C:4]([NH2:6])[N:5]=2)=[N:14]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 5742Guanidine HydrochlorideHCID 25517Ammonium ChlorideHCID 5360545SodiumHCID 22260629(2E)-3-(Dimethylamino)-1-(1H-indazol-3-yl)-2-propen-1-one

生成物 1

HCID 22260979HCID 22260979、化合物収率 65.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A total of 20 mg of metallic sodium was dissolved in 5 ml of dry ethanol. To the resulting solution were added 76 mg of guanidine hydrochloride and 85 mg of (E)-3-(dimethylamino)-1-(1H-3-indazolyl)-2-propen-1-one, followed by heating under reflux for 12 hours. To the reaction mixture was added aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was purified and separated by silica gel column chromatography (ethyl acetate:hexane=7:5), to give 55 mg of the title compound as a colorless powder.

後処理

  1. temperatureby heating
  2. temperatureunder reflux for 12 hours
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe organic layer was washed with water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated
  7. customThe residue was purified
  8. customseparated by silica gel column chromatography (ethyl acetate:hexane=7:5)

出典と根拠

ORDレコード
ord-5b3bc6c905704f6ba4da1fa785ea68a4
出典データセット
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06982274B2

反応ノート

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