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HRID 30402생성일: 2026년 10월 24일

Isatoic Anhydride → 2-amino-N'-(4-chlorophenyl)benzohydrazide

https://huagongshe.com/ko/reaction/30402

반응식

참여 물질

역할이름HCID투입량
반응물Isatoic AnhydrideHCID 8359—
반응물Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
반응물DiisopropylethylamineHCID 81531—
용매EthanolHCID 702—
생성물2-amino-N'-(4-chlorophenyl)benzohydrazideHCID 2182059950%

반응 단계

4-Chlorophenylhydrazine hydrochloride (2.105 g, 14.76 mmol) was suspended in EtOH (25 ml), treated with di-isopropylethylamine (2.253 ml, 12.93 mmol) and stirred for 30 minutes. Isatoic anhydride (1.918 g, 11.76 mmol) was added and the mixture was heated to reflux for 3 hours. The reaction mixture was cooled to room temperature and stirred overnight. The material was concentrated to dryness and the resulting residue was partitioned between EtOAc (˜25 ml) and 50% saturated NaCl (3×30 ml). The organic layer (also containing a small amount of emulsion which would not dissipate over 3 extractions) was dried over MgSO4 and concentrated to an orange solid. The material was triturated with EtOAc, filtered and rinsed with additional EtOAc. The filtrate was concentrated to dryness and treated with DCM (dichloromethane). The mixture was stirred overnight. The mixture was filtered, rinsed with DCM and the solid dried to provide 1.538 g (50%) of 2-amino-benzoic acid N′-(4-chloro-phenyl)-hydrazide (Intermediate 40) as a mauve-colored solid. MS (APCI): (M+1)=262.1, (M−1)=260.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423054B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-fafd3337a3cd457db53e4e5251973741
출처 메모uspto-grants-2008_09