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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487248생성일: 2026년 10월 24일

Methanesulfonic Acid → HCID 178437841, 화합물

https://huagongshe.com/ko/reaction/487248

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물6-Methyl-2-pyridinecarboxaldehydeHCID 70737—
반응물5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
생성물HCID 178437841HCID 17843784153.3%

반응 단계

1-Cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (2.0 g, 9.0 mmol), 6-methyl-2-pyridinecarboxaldehyde (2.2 g, 18.0 mmol), methanesulfonic acid (0.5 ml) and xylenes (80 ml) were combined and heated to reflux for 24 hours. The solvents were removed in vacuo, ethanol was added and the solvents were removed in vacuo. The residue was partitioned between 10% K2CO3 and chloroform, the organic layer was separated and the aqueous layer was extracted with chloroform (3×200 ml). The combined organic layers were concentrated in vacuo, redissolved in dichloromethane and combined with silica gel (40 g). The slurry was air dried for 3 hours, and placed on a silica gel column (150 g). Elution with ether and concentration of the solvent in vacuo and drying the residue at 40° C. in high vacuum for 6 hours afforded 1.55 g (53%) of 1-cyclopentyl-3-ethyl-6-(6-methyl-2-pyridyl)-pyrazolo[3,4-d]pyrimidin-4-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05294612
출처 데이터셋uspto-grants-1994_03
ORD IDord-36920c4b9c2e4c60843c0856108c7a55
출처 메모uspto-grants-1994_03