돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 508653생성일: 2026년 10월 23일

2-Chloro-5-nitropyrimidine → HCID 53260086, 화합물

https://huagongshe.com/ko/reaction/508653

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-5-nitropyrimidineHCID 82544—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 12134904HCID 12134904—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물HCID 53260086HCID 5326008619%

반응 조건

온도90 °C

반응 단계

To a solution of 3-(1-adamantyl)-4-benzyloxyphenylboronic acid (1) (833 g, 2.3 mmol) and 2-chloro-5-nitropyrimidine (2) (320 mg, 2.00 mmol) in degassed toluene (15 mL) was added tetrakis(triphenylphosphine)palladium (347 mg, 0.300 mmol), NaHCO3 (336 mg, 4.00 mmol) and degassed H2O (3 mL). The mixture was heated at reflux (90° C. oil-bath) for 24 h, cooled to room temperature and extracted with EtOAc (180 mL). The extract was washed (H2O and brine) and dried. After solvent removal at reduced pressure, the residue was chromatographed (3% EtOAc/hexane) to give 165 mg (19%) of 2-[3-(1-adamantyl)-4-benzyloxyphenyl]-5-nitropyrimidine as a yellow solid, mp 206° C. (dec). IR 2902, 1405, 1179 cm−1; 1H NMR (CDCl3) δ 1.76 (bs, 6H, AdCH2), 2.09 (bs, 311, AdCH), 2.22 (m, 6H, AdCH2), 5.24 (s, 2H, C6H5CH2), 7.07 (d, J=8.7 Hz, 1H, 5′-ArH), 7.34-7.53 (m, 5H, C6H5), 8.40 (dd, J=8.7 Hz, 2.4 Hz, 1H, 6′-ArH), 8.51 (d, J=2.4 Hz, 1H, 2′-ArH), 9.46 ppm (s, 2H, 4-ArH, 6-ArH). HRMS calcd C27H27N3O3 [M+H]+ 442.2125. found 442.2137.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096544B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-ff0bd70eb6a4423f90afdcec38042ca9
출처 메모uspto-grants-2015_08