돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217004생성일: 2026년 10월 25일

Diisopropylethylamine → HCID 178422437, 화합물

https://huagongshe.com/reaction/217004

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물Cyclopropyl methyl hydroxylamine hydrochlorideHCID 21114231—
반응물HCID 178422438HCID 178422438—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물HCID 178422437HCID 17842243745%

반응 단계

7-Fluoro-6-(4-bromo-2-methyl-phenylamino)-1H-benzoimidazole-5-carboxylic acid 10a (48 mg, 0.132 mmol) is dissolved in 1:1 THF: methylene chloride (1 mL) and Hunig's base (0.23 μL, 1.32 mmol) is added followed by PyBOP (82 mg, 0.158 mmol). After a few minutes, cyclopropyl methyl hydroxylamine hydrochloride (20 mg, 0.158 mmol) (WO 00/42022) is added. After the reaction is complete, the mixture is partitioned between methylene chloride and saturated NaHCO3 solution. The layers are separated and the organic layer is washed with saturated NaHCO3 and brine. The organic layer is dried (Na2SO4) and concentrated under reduced pressure. After purification by FCC (elute with 20:1 methylene chloride/MeOH), 25 mg (45%) of pure desired product is isolated: MS ESI (+) m/z 435, 433 (M+1 Br pattern) detected; MS ESI (−) m/z 433, 431 (M−1 Br pattern) detected; 1H NMR (400 MHz, CDCl3) δ 8.15 (s, 1H), 8.02 (s, 1H), 7.28 (s, 1H), 7.43 (d, 1H), 7.07 (dd, 1H), 6.36 (m, 1H), 3.70 (d, 2H), 2.38 (s, 3H), 0.86 (m, 1H), 0.41 (m, 2H), 0.13 (m, 2H); 19F NMR (376 MHz, CDCl3)-134.05 (s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193231B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-5a2012dc2f5b4ec7832005c42381ce53
출처 메모uspto-grants-2012_06