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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 901150생성일: 2026년 10월 25일

Ethyl Acetate → 4-[(4-Benzyloxy-3-chloro-benzyl)-[1,2,4]triazol-4-yl-amino]-benzonitrile

https://huagongshe.com/reaction/901150

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물Benzonitrile, 4-(4H-1,2,4-triazol-4-ylamino)-HCID 10307909—
반응물1-Benzyloxy-4-bromomethyl-2-chloro-benzeneHCID 10968968—
용매DimethylformamideHCID 6228—
생성물4-[(4-Benzyloxy-3-chloro-benzyl)-[1,2,4]triazol-4-yl-amino]-benzonitrileHCID 21976889—

반응 단계

Sodium hydride (60%, 200 mg, 5.0 mmol) was added to a solution of 4-([1,2,4]triazol-4-ylamino)-benzonitrile (926 mg, 5.0 mmol) in DMF (20 mL) at r.t. The mixture was stirred for 1 hour at this temperature and 1-benzyloxy-4-bromomethyl-2-chloro-benzene (CAB02128, 1.56 g, 5.0 mmol) was added. The reaction mixture was stirred overnight and ethyl acetate (75 mL) was added. The mixture was transferred into a separation funnel and washed with water (two times 100 mL) and brine (20 mL). The organic layer was dried over sodium sulphate and concentrated under reduced pressure. The residue was suspended in 2-propanol (20 mL) and heated to reflux for 5 minutes. The white solid was filtered off after cooling to room temperature and dried under high vacuum. Yield: 1.38 g (66%). 1H-NMR (400 MHz, d6-DMSO) δ=4.99 (s, 2H), 5.17 (s, 2H), 6.76 (d, J=9.0 Hz, 2H), 7.16 (d, J−8.6 Hz, 1H), 7.20 (dd, J=8.6, 2.2 Hz, 1H), 7.32-7.47 (m, 6H), 7.76 (d, J=9.0 Hz, 2H), 8.81 (s, 2H). LRMS (FAB+): 416.1 (100, [M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361677B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-8b0eb1bdabc54f1c86d2ffb0cde38dbe
출처 메모uspto-grants-2008_04