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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1167566생성일: 2026년 10월 25일

tert-Butanol → N-benzyloxycarbonyl-5-aminomethyl-4-(4-pyridyl)-3-(4-fluorophenyl)pyrazole

https://huagongshe.com/reaction/1167566

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물TetrahydrofuranHCID 8028—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물N-benzyloxycarbonyl-glycyl-N-hydroxysuccinimideHCID 22037183—
반응물1,1-dimethylethyl 4-[5-(4-fluorophenyl)-4-(4-pyridinyl)-1H-pyrazol-3-yl]-1-piperazinecarboxylateHCID 22037321—
반응물Potassium tert-butoxideHCID 23665647—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물N-benzyloxycarbonyl-5-aminomethyl-4-(4-pyridyl)-3-(4-fluorophenyl)pyrazoleHCID 69409299—

반응 단계

A 3 L round bottom flask fitted with a mechanical stirrer, N2 inlet and an addition funnel was was charged wtih 557 mL (0.56 mol) of 1 M t-BuOK in THF and 53 mL (0.56 mol) of t-BuOH. The ketone, 1 (60 g, 0.28 mol) was dissolved in 600 mL of THF and added to the stirred mixture at room temperature. A yellow precipitate formed and the mixture was stirred for 1 h. N-benzyloxycarbonyl-glycinyl N-hydroxysuccinimide (128.6 g, 0.42 mol) was dissolved in 600 mL of THF and added dropwise at r.t. over 1 h. The mixture was stirred for another 5 minutes and 150 mL of water was added. The pH was adjusted to 6.7 with 70 mL of AcOH. Hydrazine monohydrate (41 mL in 100 mL of water) was added via an addition funnel. The mixture was stirred for 1 h and was diluted with 500 mL of water and 500 mL of ethyl acetate. The biphasic mixture was transferred to a sep funnel and the layers were separated. The aqueous layer was extracted with EtOAc (3×300 mL). The organic layer was dried (Na2SO4), filtered and evaporated to leave 157 g of a crude reddish oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06617324B1
출처 데이터셋uspto-grants-2003_09
ORD IDord-16ac67abf21f439ca2c6dc20851ec3b4
출처 메모uspto-grants-2003_09