돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1499102생성일: 2026년 10월 25일

N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzene-1-sulfonamide → HCID 117942080, 화합물

https://huagongshe.com/reaction/1499102

반응식

참여 물질

역할이름HCID투입량
반응물N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzene-1-sulfonamideHCID 2734565—
반응물Potassium FormateHCID 2735122—
반응물1-(4-Bromo-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanoneHCID 117942112—
촉매HCID 178477776HCID 178477776—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물HCID 117942080HCID 117942080—

반응 조건

온도50 °C

반응 단계

Pentamethylcyclopentadienyl iridium (III) chloride dimer (CAS#12354-84-6) (10.4 mg) and (1R,2R)-(−)-N-(4-toluene sulfonyl)-1,2-diphenyl ethylene diamine (CAS#144222-34-4) (9.2 mg) were combined in water (120 mL), then heated to 50° C. for 5 h to provide the “Iridium complex.” 1-[4-Bromo-2-(3-methyl-1H-pyrazol-1-yl)phenyl]-2,2,2-trifluoroethanone (16 g, 48 mmol) was dissolved in acetonitrile (120 mL) to which the Iridium complex and potassium formate (3.1 g, 3.7 mmol) were added. The reaction mixture was heated to 50° C. for 8 h. The reaction mixture was then cooled to RT, partitioned between water and EtOAc, and extracted. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Recrystallization from hot heptane (200 mL) provided the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09199994B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-89e44f85a3e4496ca1b80e58d5cb93fa
출처 메모uspto-grants-2015_12