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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2068413생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → 3-iodo-4-methyl-N-(1-(pyridin-2-yl)cyclopropyl)benzamide

https://huagongshe.com/reaction/2068413

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물3-Iodo-4-methylbenzoic acidHCID 621640—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-(Pyridin-2-yl)cyclopropanamineHCID 11105409—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물3-iodo-4-methyl-N-(1-(pyridin-2-yl)cyclopropyl)benzamideHCID 67217666—

반응 단계

3-Iodo-4-methylbenzoic acid (2.5 g, 9.5 mmol, 1 eq), 1-(pyridin-2-yl)cyclopropanamine (1.41 g, 10.4 mmol, 1.1 eq), EDCI.HCl (2.1 g, 11.4 mmol, 1.2 eq), HOBT (1.5 g, 11.4 mmol, 1.2 eq) and DIPEA (4.9 ml, 28.62 mmol, 3 eq) were dissolved in DCM and the above solution was stirred at room temperature for 18 h. Water was added and product was extracted with DCM. The organic layer was concentrated and the crude product crystallized using dichloromethane and hexane. Yield: 2.3 g (55%). 1HNMR (400 MHz, DMSO-d6): δ 1.26 (m, 2H), 1.53 (m, 2H), 2.43 (s, 3H), 7.13 (m, 1H), 7.29 (d, J=8.00 Hz, 1H), 7.44 (d, 1H), 7.67 (t, J=3.46 Hz, 1H), 7.87 (d, J=3.24 Hz, 1H), 8.38 (s, 1H), 8.44 (d, J=1.10 Hz, 1H), 9.29 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08293909B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-6405fd1cc2ae4543ba906786ef7a7aad
출처 메모uspto-grants-2012_10