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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1724149생성일: 2026년 10월 26일

Triethylamine → Benzoic acid N'-(2-9H-fluoren-9-yl-acetyl)-N'-isopropyl-hydrazide

https://huagongshe.com/reaction/1724149

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-Benzoyl-2-isopropylhydrazineHCID 18869—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Fluorene-9-acetic acidHCID 94852—
용매DimethylformamideHCID 6228—
생성물Benzoic acid N'-(2-9H-fluoren-9-yl-acetyl)-N'-isopropyl-hydrazideHCID 5756011740.4%

반응 단계

A solution of 9-fluoreneacetic acid (126 mg, 0.56 mmoles) and benzoic acid N′-isopropyl-hydrazide (100 mg, 0.56 mmoles) in DMF (5 mL) was treated with triethylamine (0.23 mL, 1.68 mmol), HOBT (91 mg, 0.67 mmoles) and EDCI (129 mg, 0.67 mmol) at room temperature for 72 h. The reaction mixture was partitioned between water and dichloromethane. The organic layer was washed with water and brine, then dried over sodium sulfate, filtered and concentrated. The crude was absorbed on silica and purified on a silica gel column with a 10-30% ethyl acetate/hexanes gradient to afford the product as a solid (87 mg, 40%). LC-MS m/e 385.19 (M+H+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07485752B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-3d7adb47e45b4550bc5045491a132aa7
출처 메모uspto-grants-2009_02