戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 41952作成日:2026年10月25日

Pyridine → (E)-N-(2,1,3-benzoxadiazol-5-ylmethoxy)-5,6-dimethoxy-2,3-dihydroinden-1-imine

https://huagongshe.com/reaction/41952

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物5,6-Dimethoxy-1-indanoneHCID 75018—
反応物O-(benzo[c][1,2,5]oxadiazol-5-ylmethyl)hydroxylamine hydrochlorideHCID 66760966—
反応物(E)-6,7-dimethoxy-N-[(4-nitrophenyl)methoxy]-3,4-dihydro-2H-naphthalen-1-imineHCID 87138450—
溶媒EthanolHCID 702—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物(E)-N-(2,1,3-benzoxadiazol-5-ylmethoxy)-5,6-dimethoxy-2,3-dihydroinden-1-imineHCID 8713864285.3%

反応手順

5,6-Dimethoxy-1-indanone (38 mg, 0.19 mmol) was subjected to reaction with O-(benzo[c][1,2,5]oxadiazol-5-ylmethyl)hydroxylamine hydrochloride (39 mg, 0.19 mmol) in ethanol (2 mL) and pyridine (0.2 mL, 2.58 mmol) under the same conditions as described for (E)-6,7-dimethoxy-3,4-dihydronaphthalen-1(2H)-one O-4-nitrobenzyl oxime. Subjection of the material obtained on work up to flash chromatography (3:7 v/v ethyl acetate/hexane elution) afforded the title compound as off-white crystals (55 mg, 82%), m.p. 163-166° C., Rf 0.4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536157B2
出典データセットuspto-grants-2013_09
ORD IDord-79490ee6dbb0457fbbbf3dc97b5fd167
出典メモuspto-grants-2013_09