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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 457335생성일: 2026년 10월 26일

8-{[(2-chloropyridin-3-yl)carbonyl]amino}-1-(4-ethynylphenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide → 8-{[(2-chloropyridin-3-yl)carbonyl]amino}-1-(4-vinylphenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide

https://huagongshe.com/reaction/457335

반응식

참여 물질

역할이름HCID투입량
반응물8-{[(2-chloropyridin-3-yl)carbonyl]amino}-1-(4-ethynylphenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxamideHCID 22291546—
용매N,N-dimethylformamide; methylsulfinylmethaneHCID 3013483—
생성물8-{[(2-chloropyridin-3-yl)carbonyl]amino}-1-(4-vinylphenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxamideHCID 2229169247%

반응 단계

A solution of 8-{[(2-chloropyridin-3-yl)carbonyl]amino}-1-(4-ethynylphenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide (557 mg, 1.19 mmol) in DMF-DMSO (20 mL-1 mL) was treated at RT with H2 (5 psi) and Pd—CaSO4 (5%, 100 mg) for 12 min. The mixture was filtered through celite pad, concentrated and added water. The solid product was collected via filtration, washed with water and ether, and dried to give product (262 mg, 47%). 1H NMR was consistent with its structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186743B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-a8d45760e38e424fbd2163fe3a51c169
출처 메모uspto-grants-2007_03