戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 255239作成日:2026年10月25日

Sodium hydride → tert-Butyl{1-[2-(6-bromo-3-oxo-2,3-dihydro-4H-pyrido[3,2-b][1,4]oxazin-4-yl)ethyl]piperidin-4-yl}carbamate

https://huagongshe.com/reaction/255239

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物6-Bromo-2H-pyrido[3,2-B][1,4]oxazin-3(4H)-oneHCID 21873772—
反応物2-(4-((Tert-butoxycarbonyl)amino)piperidin-1-yl)ethyl methanesulfonateHCID 56834478—
反応物tert-butyl {1-[2-(7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl]piperidin-4-yl}carbamateHCID 59371209—
生成物tert-Butyl{1-[2-(6-bromo-3-oxo-2,3-dihydro-4H-pyrido[3,2-b][1,4]oxazin-4-yl)ethyl]piperidin-4-yl}carbamateHCID 8664262092%

反応手順

6-Bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one (WO 2004/058144) (935 mg, 4.08 mmol) was deprotonated with sodium hydride and alkylated with 2-{4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}ethyl methanesulfonate (Intermediate 6) (5.6 mmol) as described for Intermediate 2, but chromatography was omitted, to give the product as a solid in 92% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07875715B2
出典データセットuspto-grants-2011_01
ORD IDord-0c0305fd4be142aa9036ae1fb2f19d46
出典メモuspto-grants-2011_01