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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551291생성일: 2026년 10월 26일

Diisopropylethylamine → HCID 67194128, 화합물

https://huagongshe.com/reaction/551291

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-(2-Phenyleth-1-Ynyl)Nicotinic AcidHCID 2779236—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물1-(3-Cyanophenyl)piperazineHCID 11480902—
용매DimethylformamideHCID 6228—
생성물HCID 67194128HCID 6719412852%

반응 단계

A solution of 5-phenylethynyl-pyridine-3-carboxylic acid (0.4 g, 1.8 mmol) in anhydrous dimethylformamide (3 ml) is treated with HATU (0.7 g, 1.8 mmol) and diisopropylethylamine (0.6 ml, 3.3 mmol). The reaction mixture is stirred 10 mins. at ambient temperature before being treated with a solution of 1-(3-cyanophenyl)piperazine (0.3 g, 1.6 mmol) in dimethylformamide (5 ml). The reaction mixture is stirred at ambient temperature for 18 hours, concentrated under vacuum and the residue partitioned between dichloromethane (2×40 ml) and saturated aqueous sodium bicarbonate (40 ml). The organic layer is dried (magnesium sulfate), concentrated under vacuum and the residue chromatographed on silica gel (ethyl acetate) to give the title compound as a yellow oil (0.33 g). 1H NMR (CDCl3, 500 MHz) δ8.82 (s, 1H), 8.61 (s, 1H), 7.90 (s, 1H), 7.58 (m, 2H), 7.39 (m, 4H), 7.16 (m, 3H), 3.95 (br m, 2H), 3.63 (br m, 2H), 3.30 (br m, 4H), EI MS M++H: 393.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947684B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-ac3ec2b55b6a4f5bb096505160cd6c1c
출처 메모uspto-grants-2011_05