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HRID 1247006作成日:2026年10月26日

Sodium Sulfite → Benzyl (S)-2-(7-bromo-6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamate

https://huagongshe.com/reaction/1247006

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium SulfiteHCID 24437—
反応物N-bromobutanimideHCID 67184—
反応物Benzyl (S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamateHCID 135487328—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl (S)-2-(7-bromo-6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamateHCID 136207273—

反応手順

A solution of benzyl (S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamate (3.00 g, 9.23 mmol) from Step A in tetrahydrofuran (30 mL) was cooled in an ice bath, small portions of N-bromosuccinimide (1.64 g, 9.23 mmol) were added and the mixture was stirred for a few minutes followed by the addition of a saturated aqueous solution of sodium sulfite (150 mL). The mixture was extracted with ethyl acetate (2×100 mL). The combined extracts were dried over magnesium sulfate, filtered, and evaporated to a white solid (3.76 g): mp 40° C.; LC/MS m/z 404/406.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07129257B1
出典データセットuspto-grants-2006_10
ORD IDord-96449b0cdb6144c5a444c2498fa9eb97
出典メモuspto-grants-2006_10