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HRID 364281作成日:2026年10月26日

Dimethylformamide → HCID 178485208、化合物

https://huagongshe.com/reaction/364281

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1,1,1-Trifluoro-2-isothiocyanatoethaneHCID 13883777—
反応物HCID 178485209HCID 178485209—
生成物HCID 178485208HCID 178485208—

反応手順

A mixture of 2,4-diamino-6-[5-(2-methanesulphonyl-3-methylguanidino)pentyl]-1,3,5-triazine (0.4 g.), 2,2,2-trifluoroethylisothiocyanate (0.4 g.) and dimethylformamide (0.5 ml.) was heated at 120° for 1 hour and then at 60° for 18 hours. The mixture was evaporated to dryness, the residue partitioned between water and ethyl acetate, and the ethyl phase was separated, dried, and evaporated to dryness. The residue was dissolved in saturated ethanolic ammonia (10 ml.) and the solution treated with yellow mercuric oxide (0.5 g.). The mixture was stirred at room temperature for 18 hours, filtered and the filtrate evaporated to dryness. The residue was purified by chromatography using ethyl acetate/methanol/ammonia 6:1:0.5 v/v/v as developing solvent to give 2-amino-4-[2-(2,2,2-trifluoroethyl)guanidino]-6-[5-(2-methanesulphonyl-3-methylguanidino)pentyl]-1,3,5-triazine (0.07 g.) characterised as the bishydrogen maleate, m.p. 131°-133° after recrystallisation from acetone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04604465
出典データセットuspto-grants-1986_08
ORD IDord-cbb8e32765b148da8178a6068fd1ba9d
出典メモuspto-grants-1986_08