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HRID 1091639作成日:2026年10月25日

Triethylamine → N-(3,4-diaminophenyl)-2-(diethylamino)acetamide

https://huagongshe.com/reaction/1091639

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-oneHCID 4293995—
反応物2-Nitro-4-phenylenediamineHCID 4338370—
反応物Glycine, N,N-diethyl-, sodium salt (1:1)HCID 23670834—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒AcetonitrileHCID 6342—
生成物N-(3,4-diaminophenyl)-2-(diethylamino)acetamideHCID 66593690—

反応手順

2-Nitrobenzene-1,4-diamine (1.55 g, 10.1 mmol), N,N-diethylglycine sodium salt (1.61 g, 10.6 mmol) and DEPBT (3.02 g, 10.0 mmol) were suspended in acetonitrile (75 mL). Triethylamine (2.8 mL, 20.0 mmol) was added and the solution stirred overnight at room temperature. The brown precipitate which was formed was filtered and discarded. The filtrate was concentrated and the residue partitioned between EA and saturated aqueous sodium bicarbonate. The organic phase was washed with water and then with brine, dried over sodium sulfate, and the solvent removed under reduced pressure. The residue was dissolved in ethanol (50 mL) and hydrogenated at atmospheric pressure with 10% palladium on charcoal (1.0 g, 0.9 mmol) at room temperature overnight. Filtration and concentration under reduced pressure gave N-(3,4-diaminophenyl)-2-(diethylamino)acetamide as a light brown semi-solid, which solidified and turned blue on standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129396B2
出典データセットuspto-grants-2012_03
ORD IDord-bd23b24b0e704bdcb05f4b922f251601
出典メモuspto-grants-2012_03