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HRID 38849作成日:2026年10月24日

Sodium Iodide → 6-bromo-4-{5-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylmethyl]-1,3,4-oxadiazol-2-yl}-1-(phenylsulfonyl)-1H-indazole

https://huagongshe.com/ja/reaction/38849

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物DiisopropylethylamineHCID 81531—
反応物(6S)-1,4-Diazabicyclo(4.3.0)nonaneHCID 781249—
反応物6-bromo-4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-1-(phenylsulfonyl)-1H-indazoleHCID 66695668—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物6-bromo-4-{5-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylmethyl]-1,3,4-oxadiazol-2-yl}-1-(phenylsulfonyl)-1H-indazoleHCID 6669585461.2%

反応条件

温度70 °C

反応手順

6-Bromo-4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-1-(phenylsulfonyl)-1H-indazole (300 mg, 0.661 mmol) and sodium iodide (99 mg, 0.661 mmol) were weighed into a round-bottomed flask and dissolved in acetonitrile (2 ml) before (S)-1,4-diazabicyclo[4.3.0]nonane (167 mg, 1.322 mmol, available from ABCR GmbH & CO.KG) and DIPEA (0.231 ml, 1.322 mmol) were added. The mixture was heated to 70° C. for 2 h. The mixture was cooled, diluted with DCM and washed with 2 M aqueous HCl (2 ml). The organic layer was separated by hydrophobic frit. The aqueous extracts were combined and neutralised to pH 7 with NaOH then extracted with more DCM (2×10 ml) which was combined with the other organic extracts and evaporated under a stream of nitrogen to give an orange oil. This was dissolved in DCM and loaded onto the top of a 10 g silica cartridge that was subsequently eluted with 0-15% MeOH(+1% triethylamine)/DCM over 15 mins. The appropriate fractions were combined and the solvent removed in vacuo to give the title compound as a cream solid (220 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524751B2
出典データセットuspto-grants-2013_09
ORD IDord-ed3410ad0501475e838a07c4af6e2d0b
出典メモuspto-grants-2013_09