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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1062585생성일: 2026년 10월 27일

Triethylamine → Methyl 4-[(2-amino-5-iodo-benzoylamino)-methyl]-benzoate

https://huagongshe.com/reaction/1062585

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzoic acid, 2-amino-5-iodo-HCID 72911—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Methyl 4-(aminomethyl)benzoate hydrochlorideHCID 2729253—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매DimethylformamideHCID 6228—
생성물Methyl 4-[(2-amino-5-iodo-benzoylamino)-methyl]-benzoateHCID 2228187770%

반응 단계

To a stirred solution of 15 g (74.4 mmol) of methyl 4-(aminomethyl)benzoate hydrochloride, 300 ml of dimethylformamide and 10.3 ml (7.53 g, 74.4 mmol) of triethylamine were added, at room temperature, followed by 10.06 g (74.4 mmol) of 1-hydroxybenzotriazole hydrate, 19.6 g (74.4 mmol) of 2-amino-5-iodobenzoic acid and 14.3 g (74.4 mmol) of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride. After stirring at room temperature overnight, the mixture was concentrated and the residue was dissolved in 300 ml of dichloromethane. The organic phase was washed with 150 ml H2O, 150 ml HCl 1N, and 150 ml H2O, dried over sodium sulfate and concentrated. The residue was recrystallized from 170 ml acetonitrile to afford after filtration 19.6 g of the desired product (yield: 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06962922B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-fc77ddb5ab5549c5b7e3d30e19bd348e
출처 메모uspto-grants-2005_11