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HRID 277001作成日:2026年10月27日

Benzyloxyamine hydrochloride → HCID 178419047、化合物

https://huagongshe.com/reaction/277001

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyloxyamine hydrochlorideHCID 102312—
反応物5'-Bromo-2'-(methylthio)spiro[cyclohexane-1,3'-[3H]indole]HCID 21986266—
溶媒MethanolHCID 887—
生成物HCID 178419047HCID 178419047—

反応条件

温度45 °C

反応手順

5′-Bromo-2′-(methylthio)spiro[cyclohexane-1,3′-[3H]indole] (9.0 g, 28.98 mmol) and O-benzylhydroxylamine hydrochloride (13.8 g, 86.9 mmol) were combined in methanol (150 mL) and heated to 45° C. for 6 hours. Methanol was evaporated in vacuo. Ethyl acetate was added to the residue and this mixture was washed with ammonium chloride solution. Ethyl acetate was dried over magnesium sulfate, ethyl acetate collected evaporated in vacuo and the residue was flash chromatographed on alumina 90 (9:1 Hexane/EtOAc) to the desired product (6.5 g, 60%). 1H NMR (DMSO-d6, 300 MHz) δ 1.38-1.70 (m, 8H), 1.92-2.06 (m, 2H), 5.06 (s, 2H), 6.71 (d, 1H, J=8.26 Hz), 7.22-7.43 (m, 7H), 9.62 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355648B1
出典データセットuspto-grants-2002_03
ORD IDord-e9cebc96061443debf3b03d4c369ac60
出典メモuspto-grants-2002_03