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HRID 517554作成日:2026年10月25日

1-Hydroxybenzotriazole → 5-(4-(3-Bromobenzyl)-5-methylthiazol-2-yl)-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/517554

反応式

関与物質

役割名称HCID仕込み量
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-(Trifluoromethoxy)benzamidoximeHCID 2733309—
反応物Ethyl 4-(3-bromobenzyl)-5-methylthiazole-2-carboxylateHCID 86711493—
触媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物5-(4-(3-Bromobenzyl)-5-methylthiazol-2-yl)-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazoleHCID 8671149568%

反応手順

A solution of ethyl 4-(3-bromobenzyl)-5-methylthiazole-2-carboxylate (0.06 mmol, crude from previous step), EDC.HCl (12 mg, 0.1 mmol) and HOBT (10 mg, 0.1 mmol) in DMF (0.4 mL) was stirred at RT for 30 min. N-hydroxy-4-(trifluoromethoxy)benzimidamide (15 mg, 0.07 mmol) was added and the reaction mixture was stirred for 1 h at RT. DMF (2 mL) was added to the mixture with 2 drops of AcOH. The mixture was subsequently heated to 140° C. for additional 2 h and then cooled to RT, diluted with H2O and taken into EtOAc. The organic layer was washed with NaHCO3, concentrated, and purified by silica gel column chromatography(0-45% EtOAc/Hexane) to give the titled compound (19 mg, 68%). MS (ES+) C20H13BrF3N3O2S requires: 495, 497, found: 496, 498 [M+H]+(1:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115120B2
出典データセットuspto-grants-2015_08
ORD IDord-a2786c6924934814a4cea2356ca0a92b
出典メモuspto-grants-2015_08