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HRID 1992404作成日:2026年10月27日

Sodium Carbonate → 4-Cyano-N-{2-[7-(1-methyl-1H-indol-3-ylmethyl)-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl]-ethyl}-benzenesulfonamide

https://huagongshe.com/reaction/1992404

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物1-Methyl-1H-indole-3-carbaldehydeHCID 87894—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物4-cyano-N-[2-(9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl)ethyl]-benzenesulfonamideHCID 68518957—
溶媒1,2-DichloroethaneHCID 11—
生成物4-Cyano-N-{2-[7-(1-methyl-1H-indol-3-ylmethyl)-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl]-ethyl}-benzenesulfonamideHCID 1156204352.8%

反応手順

A mixture of 4-cyano-N-[2-(9-oxa-3,7-diaza-bicyclo[3.3.1]non-3-yl)-ethyl]-benzenesulfonamide (0.101 g, 0.30 mmol) and 1-methyl-1H-indole-3-carbaldehyde (0.081 g, 0.51 mmol) in 1,2-dichloroethane (4 mL) was agitated for 1.5 hours at room temperature. Sodium triacetoxyborohydride (0.216 g, 1.02 mmol) was added and resulting mixture was agitated over night at room temperature. An aqueous solution of Na2CO3 (3 mL) was added and the aqueous layer was extracted with dichloromethane (3×4 mL). The combined organic layers were concentrated in vacuo and the crude product was purified by chromatography on silica gel using methanol saturated with ammonia in dichloromethane as eluent, which afforded 76 mg (52.8%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07648985B2
出典データセットuspto-grants-2010_01
ORD IDord-61ae9431537d42e7931650173a6d0410
出典メモuspto-grants-2010_01