Thionyl Chloride → HCID 20511269、化合物

HRID 1578287ノート

反応式

HRID 1578287 の反応式
[CH3:1][N:2]1[C:6]([CH2:7][C:8](O)=[S:9])=[N:5][N:4]=[N:3]1.S(Cl)([Cl:13])=O>C1C=CC=CC=1.CN(C)C=O>[CH3:1][N:2]1[C:6]([CH2:7][C:8]([Cl:13])=[S:9])=[N:5][N:4]=[N:3]1

参加物

5

実験手順

To a suspension of (1-methyl-1H-tetrazol-5-yl)-thioacetic acid (10 g) in dried benzene (100 ml) were added a solution of thionyl chloride (10.2 g) in dried benzene (30 ml) and dimethylformamide (1 drop) in turn at room temperature, and the mixture was refluxed for 1 hour. After the reaction, the solvent was distilled off to give crystals of (1-methyl-1H-tetrazol-5-yl)thioacetyl chloride. To a solution of 3,4-dibenzyloxyphenethylamine (9.3 g) in a mixture of dried benzene (90 ml) and dried chloroform (10 ml) was firstly added triethylamine (3.66 g) and then was dropwise added over 20 minutes under stirring and ice cooling a solution of the above obtained (1-methyl-1H-tetrazol-5-yl)-thioacetyl chloride in a mixture of dried benzene (50 ml) and dried chloroform (5 ml). The mixture was stirred for 30 minutes at the same temperature and for 30 minutes at room temperature. The solvent was distilled off and the residue was dissolved in chloroform. The solution was in turn washed with 5% hydrochloric acid, water, dilute sodium bicarbonate aqueous solution and water and dried. The solvent was distilled off and the residue was crystallized from ether to give N-(3,4-dibenzyloxyphenethyl)-(1-methyl-1H-tetrazol-5-yl)-thioacetamide (10.7 g), mp 110° C.

後処理

  1. temperaturethe mixture was refluxed for 1 hour
  2. customAfter the reaction
  3. distillationthe solvent was distilled off

出典と根拠

ORDレコード
ord-eda169c828ac4ccf99b2a4d95e7c7093
出典データセット
uspto-grants-1981_09
特許番号
US04292320

反応ノート

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