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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2205111생성일: 2026년 10월 26일

Hydrochloric Acid → 3-(Benzo[d][1,3]dioxol-5-yl)-2-phenylquinoxaline-6-carboxylic acid

https://huagongshe.com/reaction/2205111

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물TricyclohexylphosphineHCID 75806—
반응물2,3-Methylenedioxyphenyl boronic acidHCID 4192659—
반응물Methyl 3-bromo-2-phenylquinoxaline-6-carboxylateHCID 86667202—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물3-(Benzo[d][1,3]dioxol-5-yl)-2-phenylquinoxaline-6-carboxylic acidHCID 8671811041.1%

반응 단계

A suspension of methyl 3-bromo-2-phenylquinoxaline-6-carboxylate (80 mg, 0.23 mmol, 1.00 equiv), benzo[d][1,3]dioxol-4-ylboronic acid (59 mg, 0.36 mmol, 1.50 equiv), tricyclohexylphosphine (9 mg, 0.03 mmol, 0.14 equiv), Pd2(dba)3 (13 mg, 0.01 mmol, 0.06 equiv), and K3PO4 (149 mg, 0.80 mmol, 3.00 equiv). in dioxane/H2O (1/0.5 mL) in a 10-mL sealed tube was allowed to react, with stifling, overnight at 95° C. The pH value of the solution was adjusted to 7 with HCl (1N). Purification via silica gel column (dichloromethane:methanol (1:10)) afforded 35 mg (40%) of 3-(benzo[d][1,3]dioxol-5-yl)-2-phenylquinoxaline-6-carboxylic acid as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09370522B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-320bf4d8c83d42f4b42d168b923f589e
출처 메모uspto-grants-2016_06