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HRID 1768089作成日:2026年10月26日

Benzenesulfinic acid → 5-amino-1-(chloromethyl)-3-((5,6,7-trimethoxyindol-2-yl)carbonyl)-1,2-dihydro-3H-benz(e)indole

https://huagongshe.com/reaction/1768089

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfinic acidHCID 12057—
反応物Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
反応物SodiumHCID 5360545—
反応物N-allyl-1-(chloromethyl)-3-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-1,2-dihydro-3H-benzo[e]indol-5-amineHCID 9806196—
触媒HCID 178418397HCID 178418397—
溶媒DichloromethaneHCID 6344—
生成物5-amino-1-(chloromethyl)-3-((5,6,7-trimethoxyindol-2-yl)carbonyl)-1,2-dihydro-3H-benz(e)indoleHCID 39170080%

反応手順

Benzenesulfinic acid, sodium salt (25 mg, 0.15 mmol) and camphorsulfonic acid (40 mg, 0.17 mmol) were added to a solution of 10a (30 mg, 0.059 mmol) in dichloromethane (5 mL). Pd(Ph3P)4 (5 mg, 0.004 mmol) was added and the reaction mixture was stirred at an ambient temperature for 30 min. The mixture was purified directly via a silica gel column. Elution with EtOAc/petroleum ether (1:1) gave 1-(chloromethyl)-3-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-1,2-dihydro-3H-benzo[e]indol-5-amine (11a) (22 mg, 80%), spectroscopically identical to an authentic sample (Atwell et al., J. Org Chem., 1998, 63, 9414).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07235578B2
出典データセットuspto-grants-2007_06
ORD IDord-8b7c7778a33449fcb86436e46f8aedca
出典メモuspto-grants-2007_06