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Sodium Hydroxide → 6-Methyl-4-(3-nitrophenyl)-2-phenyl-5-thioureidomethylpyrimidine

HRID 4686
ノート
印刷プレビュー

反応式

HRID 4686 の反応式
C([NH:9][C:10](=[S:35])[NH:11][CH2:12][C:13]1[C:14]([C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([N+:32]([O-:34])=[O:33])[CH:27]=2)=[N:15][C:16]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[N:17][C:18]=1[CH3:19])(=O)C1C=CC=CC=1.[OH-].[Na+]>CO.O>[CH3:19][C:18]1[N:17]=[C:16]([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[N:15]=[C:14]([C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([N+:32]([O-:34])=[O:33])[CH:27]=2)[C:13]=1[CH2:12][NH:11][C:10]([NH2:9])=[S:35]
参加物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 14798Sodium HydroxideHCID 540990445-(3-Benzoylthioureidomethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine

生成物 1

HCID 201513886-Methyl-4-(3-nitrophenyl)-2-phenyl-5-thioureidomethylpyrimidine収率 95.6%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

A mixture of 5-(3-benzoylthioureidomethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (1.0 g) and sodium hydroxide (0.089 g) in methanol (20 ml) and water (10 ml) was stirred for 1 hour at a room temperature. After evaporating the solvent, water (20 ml) was added thereto and stirred for 30 minutes. The resulting precipitates were collected by filtration, washed with water and dried over phosphorous pentoxide to give 6-methyl-4-(3-nitrophenyl)-2-phenyl-5-thioureidomethylpyrimidine (0.75 g).

後処理

  1. customAfter evaporating the solvent, water (20 ml)
  2. additionwas added
  3. stirringstirred for 30 minutes
  4. customThe resulting precipitates
  5. filtrationwere collected by filtration
  6. washwashed with water
  7. dry with materialdried over phosphorous pentoxide

出典と根拠

ORDレコード
ord-f619641739a748e89b0fd89a05ea9aa1
出典データセット
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04727073

反応ノート

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