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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44624생성일: 2026년 10월 24일

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/ko/reaction/44624

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(3-bromopropyl)carbamateHCID 4460490—
반응물2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
반응물HCID 178470474HCID 178470474—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 8-anilino-2-{3-[(tert-butoxycarbonyl)amino]propyl}-4,5-dihydro-2H-pyrazolo[4,3-h]quinazoline-3-carboxylateHCID 68931717—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541429B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c9881102c10b46b195f426b54d3cf480
출처 메모uspto-grants-2013_09