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|Section2= |Section7= }} Sulfamide (IUPAC name: sulfuric diamide) is a chemical compound with the molecular structure H2NSO2NH2. Sulfamide is produced by the reaction of sulfuryl chloride with ammonia. Sulfamide was first prepared in 1838 by the French chemist Henri Victor Regnault.〔Regnault, Victor (1838) ("Sur l'acide chlorosulfurique et la sulfamide" ) (On sulfuryl chloride and sulfamide), ''Annales de chimie et de physique'', series 2, 69 : 170-184; see especially "Action de gaz ammoniac sec sur la liqueur chlorosulfurique" (Action of dry ammonia gas on liquid sulfuryl chloride), pages 176-180.〕 ==Sulfamide functional group== In organic chemistry, the term ''sulfamide'' may also refer to the functional group which consists of at least one organic group attached to a nitrogen atom of sulfamide. Symmetric sulfamides can be prepared directly from amines and sulfur dioxide gas: : In this example, the reactants are aniline, triethylamine, and iodine. Sulfur dioxide is believed to be activated through a series of intermediates: Et3N-I+-I−, Et3N-I+-I3− and Et3N+-SO2−. The sulfamide functional group is an increasingly common structural feature used in medicinal chemistry. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Sulfamide」の詳細全文を読む スポンサード リンク
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