돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513297생성일: 2026년 10월 26일

Pyrazole → tert-butyl-3-(1H-pyrazol-1-yl)benzylcarbamate

https://huagongshe.com/reaction/513297

반응식

참여 물질

역할이름HCID투입량
반응물PyrazoleHCID 1048—
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyl 3-iodobenzylcarbamateHCID 11645663—
반응물(1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamineHCID 13822957—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl-3-(1H-pyrazol-1-yl)benzylcarbamateHCID 5679198570.3%

반응 조건

온도120 °C

반응 단계

To a solution of tert-butyl-3-iodobenzylcarbamate (550 mg, 1.65 mmol) in Dioxane (1.2 mL) and DMSO (1.2 mL) was added CuI (16 mg, 0.083 mmol), (1S,2S)—N1,N2-dimethylcyclohexane-1,2-diamine (0.052 ml, 0.33 mmol), pyrazole (135 mg, 1.98 mmol) and K2CO3 (479 mg, 3.47 mmol). After stirring at 120° C. for 3 h, it was concentrated and the residue was purified by column chromatography to give tert-butyl-3-(1H-pyrazol-1-yl)benzylcarbamate (317 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102625B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-953510000c43469085ac5217a1dfbbdd
출처 메모uspto-grants-2015_08