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HRID 247123作成日:2026年10月27日

3-Nitrobenzaldehyde → 1,4-Dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-5-(3-chloromethyl-1,2,4-thiadiazol-5-yl)-4-(3-nitrophenyl)pyridine

https://huagongshe.com/reaction/247123

反応式

関与物質

役割名称HCID仕込み量
反応物3-NitrobenzaldehydeHCID 7449—
反応物5-Acetonyl-3-chloromethyl-1,2,4-oxadiazoleHCID 13824705—
反応物5-(2-Amino-1-propenyl)-3-chloromethyl-1,2,4-thiadiazoleHCID 70054050—
溶媒IsopropanolHCID 3776—
生成物1,4-Dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-5-(3-chloromethyl-1,2,4-thiadiazol-5-yl)-4-(3-nitrophenyl)pyridineHCID 13583341715.5%

反応手順

A stirred mixture of 343 mg of 5-(2-amino-1-propenyl)-3-chloromethyl-1,2,4-thiadiazole, 316 mg of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole and 273 mg of 3-nitrobenzaldehyde in 5 ml of isopropyl alcohol was heated under reflux for 10 hours. The mixture was concentrated in vacuo and the residue was chromatographed on silica gel using benzene-ethyl acetate (5:1) as eluent to give 134 mg of 1,4-dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-5-(3-chloromethyl-1,2,4-thiadiazol-5-yl)-4-(3-nitrophenyl)pyridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04705786
出典データセットuspto-grants-1987_11
ORD IDord-d2e17b014b244f50b927dd81982f8200
出典メモuspto-grants-1987_11