戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 44624作成日:2026年10月25日

tert-butyl N-(3-bromopropyl)carbamate → Ethyl 8-anilino-2-{3-[(tert-butoxycarbonyl)amino]propyl}-4,5-dihydro-2H-pyrazolo[4,3-h]quinazoline-3-carboxylate

https://huagongshe.com/reaction/44624

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-(3-bromopropyl)carbamateHCID 4460490—
反応物2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
反応物HCID 178470474HCID 178470474—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 8-anilino-2-{3-[(tert-butoxycarbonyl)amino]propyl}-4,5-dihydro-2H-pyrazolo[4,3-h]quinazoline-3-carboxylateHCID 68931717—

反応手順

500 mg of ethyl 8-anilino-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate (1.5 mmol) were dissolved in 10 mL of dry dimethylformamide and 1.63 mL of 1M lithium tert-butoxide in tetrahydrofuran were added to the cooled solution. After 30 minutes under stirring at 0° C. a solution of 432 mg of tert-butoxycarbonylaminopropyl bromide in 8 mL of dry tetrahydrofuran were added dropwise. After a night at room temperature the mixture was poured into a solution of NaH2PO4 and extracted with dichloromethane. The organic layer was then dried over Na2SO4 and the solvent evaporated, giving an oil that was treated according to the following step 7, without any further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541429B2
出典データセットuspto-grants-2013_09
ORD IDord-c9881102c10b46b195f426b54d3cf480
出典メモuspto-grants-2013_09