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Thiourea → 2-Amidinothiomethyl-5-(dimethylamino)methyl-4-methylthiophene dihydrochloride

HRID 236253
ノート
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反応式

HRID 236253 の反応式
[ClH:1].C(O)(C)C.[NH2:6][C:7]([NH2:9])=[S:8].[CH3:10][N:11]([CH2:13][C:14]1[S:18][C:17]([CH2:19]O)=[CH:16][C:15]=1[CH3:21])[CH3:12]>>[ClH:1].[ClH:1].[C:7]([S:8][CH2:19][C:17]1[S:18][C:14]([CH2:13][N:11]([CH3:12])[CH3:10])=[C:15]([CH3:21])[CH:16]=1)(=[NH:9])[NH2:6]
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 3

HCID 2723790ThioureaHCID 129265355-(Dimethylamino)methyl-4-methyl-2-thenyl alcoholHCID 21912024Isopropanol hydrochloride

生成物 1

HCID 138252712-Amidinothiomethyl-5-(dimethylamino)methyl-4-methylthiophene dihydrochloride収率 82%

実験手順

In 35 ml of 21% (by weight) hydrochloric acid-isopropanol solution was suspended 2.1 g of thiourea, and 5 g of 5-(dimethylamino)methyl-4-methyl-2-thenyl alcohol was added thereto, after which the resulting mixture was subjected to reaction under reflux for 15 hours. After the mixture was allowed to stand at room temperature, the crystals deposited were collected by filtration to obtain 7 g (yield 82%) of 2-amidinothiomethyl-5-(dimethylamino)methyl-4-methylthiophene dihydrochloride having a melting point of 212°-214° C. (decomp.).

後処理

  1. additionwas added
  2. customafter which the resulting mixture was subjected to reaction
  3. temperatureunder reflux for 15 hours
  4. customto stand at room temperature
  5. filtrationthe crystals deposited were collected by filtration

出典と根拠

ORDレコード
ord-ad877ca1536846ca8be47bb969d3317c
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04643849

反応ノート

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