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Cysteamine Hydrochloride → 3-[(2-Aminoethyl)thiomethyl]isothiazole hydrochloride

HRID 2058478
ノート
印刷プレビュー

反応式

HRID 2058478 の反応式
[ClH:1].[NH2:2][CH2:3][CH2:4][SH:5].[Na].BrC[CH2:9][C:10]1[CH:14]=[CH:13][S:12][N:11]=1>C(O)C>[ClH:1].[NH2:2][CH2:3][CH2:4][S:5][CH2:9][C:10]1[CH:14]=[CH:13][S:12][N:11]=1
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 3

HCID 9082Cysteamine HydrochlorideHCID 5360545SodiumHCID 539460223-(2-Bromoethyl)-1,2-thiazole

生成物 1

HCID 205502093-[(2-Aminoethyl)thiomethyl]isothiazole hydrochloride収率 99.7%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution was prepared by the gradual addition of cysteamine hydrochloride (2.03 g) to sodium (0.83 g) dissolved in ethanol (50 ml) with stirring at 0° under a nitrogen atmosphere. After stirring for 2 hours at 0° 3-bromoethylisothiazole (3.2 g) was added dropwise over 15 minutes at 0°, the reaction mixture subsequently being set aside overnight to room temperature. Following acidification to pH 3.5 with hydrochloric acid, concentration and re-evaporation with ethanol, the residue was dissolved in ethanol, filtered and concentrated to yield 3-[(2-aminoethyl)thiomethyl]isothiazole hydrochloride (3.5 g). This was converted directly to the free base by treatment with aqueous potassium carbonate and extraction with ether. The extracts were dried over magnesium sulphate, dried and concentrated to yield the amine base as an oil (1.56 g).

後処理

  1. additionwas added dropwise over 15 minutes at 0°
  2. concentrationwith hydrochloric acid, concentration and re-evaporation with ethanol
  3. dissolutionthe residue was dissolved in ethanol
  4. filtrationfiltered
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-2a8bc0aea5c74ea3ba48c3e0b243f642
出典データセット
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04317829

反応ノート

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