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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1631316생성일: 2026년 10월 25일

Diisopropylethylamine → HCID 67500871, 화합물

https://huagongshe.com/reaction/1631316

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물2-(2,5-Difluorophenyl)pyrrolidine, (R)-HCID 7176290—
반응물HCID 178510451HCID 178510451—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 67500871HCID 67500871—

반응 단계

A flask was charged with the product from Step A (2.80 g, 17.5 mmol), benzotriazole-1-yl-oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate (9.28 g, 21.0 mmol) and dry DMF (35 mL). The suspension was stirred at ambient temperature for 2 minutes and (R)-2-(2,5-difluorophenyl)pyrrolidine (Preparation A, 3.84 g, 21.0 mmol) and diisopropylethylamine (6.78 g, 62.5 mmol) were sequentially added (mild exotherm). The mixture was stirred at ambient temperature for 3 hours and poured into H2O (175 mL). The mixture was extracted with 50% EtOAc-hexanes and the combined organic fractions were washed sequentially with 1M HCl, H2O, 1M Na2CO3 and saturated NaCl. The solution was dried over MgSO4/activated carbon and filtered through a short SiO2 plug (350 mL course frit funnel, ¼ full of SiO2, capped with a layer of MgSO4) using 50% EtOAc-hexanes for elution. The solution was concentrated to give the title compound as a brittle white foam that was crushed to a flowing white solid and dried in vacuum (5.50 g, 97%). MS (apci) m/z=326.2 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08791123B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-8a69ea9cbd984838a8ca11f84bd75978
출처 메모uspto-grants-2014_07