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Sodium borohydride → 5-Methyl-3-(4-methylsemicarbazido)-6-phenyl-2,5-dihydro-1,2,4-triazine

HRID 2290357
ノート
印刷プレビュー

反応式

HRID 2290357 の反応式
[CH3:1][C:2]1[N:3]=[C:4]([NH:14][NH:15][C:16]([NH:18][CH3:19])=[O:17])[N:5]=[N:6][C:7]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[BH4-].[Na+]>CO>[CH3:1][CH:2]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:6][NH:5][C:4]([NH:14][NH:15][C:16]([NH:18][CH3:19])=[O:17])=[N:3]1
参加物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 4311764Sodium borohydrideHCID 20232058HCID 20232058、化合物

生成物 1

HCID 155863635-Methyl-3-(4-methylsemicarbazido)-6-phenyl-2,5-dihydro-1,2,4-triazine収率 64.8%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

5-Methyl-3-(4-methylsemicarbazido)-6-phenyl-1,2,4-triazine (3.8 g) was reacted with sodium borohydride (1.5 g) in methanol. The precipitates in the reaction mixture were collected by filtration, washed with water and with methanol, and then dissolved in dimethyl sulfoxide. To the solution was added water. The resultant precipitates were collected by filtration, washed with water and ethanol, and then dried to give pale yellow powder of 5-methyl-3-(4-methylsemicarbazido)-6-phenyl-2,5-dihydro-1,2,4-triazine (2.48 g), mp 214° C. (decomp.).

後処理

  1. customThe precipitates in the reaction mixture
  2. filtrationwere collected by filtration
  3. washwashed with water and with methanol
  4. dissolutiondissolved in dimethyl sulfoxide
  5. additionTo the solution was added water
  6. customThe resultant precipitates
  7. filtrationwere collected by filtration
  8. washwashed with water and ethanol
  9. customdried

出典と根拠

ORDレコード
ord-68e9afa51f5743f6be3c15eeb7e17e46
出典データセット
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04616014

反応ノート

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