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HRID 386819作成日:2026年10月27日

Diisopropylethylamine → 4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamide

https://huagongshe.com/reaction/386819

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Amino-1,2,5-thiadiazole-3-carboxylic acidHCID 251763—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物3-Bromo-4-fluoroanilineHCID 2779286—
溶媒Hydrochloric AcidHCID 313—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamideHCID 5855824476.8%

反応手順

A solution of 4-amino-1,2,5-thiadiazole-3-carboxylic acid (250 mg, 1.7 mmol) and 3-bromo-4-fluoroaniline (393 mg, 2.1 mmol) in N,N-dimethylformamide (5 mL) was treated with O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (784 mg, 2.1 mmol) followed by N,N-diisopropylethylamine (0.36 mL, 2.1 mmol) and stirred for 16 h. The reaction mixture was diluted with brine (50 mL) and 0.1 N HCl (100 mL) and extracted with ethyl acetate (2×150 mL). The combined organic extracts were washed with brine (50 mL), dried with sodium sulfate, filtered, and concentrated. Purification of the crude reaction mixture on silica gel gave the desired product (414 mg, 76%). LCMS for C9H7BrFN4OS(M+H)+: m/z=316.9, 318.8.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372870B2
出典データセットuspto-grants-2013_02
ORD IDord-3787938b02ad40539dce4a9fc3ff1d74
出典メモuspto-grants-2013_02