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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 627935생성일: 2026년 10월 26일

Dimethylamine, hydrochloride → 4-Amino-3-chloro-N,N-dimethylbenzamide

https://huagongshe.com/reaction/627935

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylamine, hydrochlorideHCID 10473—
반응물4-Amino-3-chlorobenzoic acidHCID 17211—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-Amino-3-chloro-N,N-dimethylbenzamideHCID 20287481100%

반응 단계

DIPEA (116 mL, 699.5 mmol) was added into a suspension of dimethylamine hydrochloride (28.51 g, 349.6 mmol) in THF (600 mL). The mixture was stirred at room temperature for 0.5 h. Then 4-amino-3-chlorobenzoic acid (30.00 g, 174.8 mmol) and HATU (86.41 g, 227.2 mmol) were added into the above suspension separately. The reaction mixture was continued to be stirred for 1.5 h. Then it was concentrated and the residue was partitioned between EtOAc (300 mL) and water (150 mL). The separated organic phase was washed with water, dried over Na2SO4 and evaporated in vacuum. The crude product was purified by silica gel chromatography, eluted with Hexanes: EtOAc=1:1 to afford 4-amino-3-chloro-N,N-dimethylbenzamide (34.72 g, yield: 89%). ESI-MS: 199.06. 1H NMR (CDCl3, 400 MHz): 0.39 (s, 1H, ArH), 7.19 (d, J=8.4 Hz, 1H, ArH), 6.74 (d, J=8.4 Hz, 1H, ArH), 4.24 (br, 2H, NH2), 3.05 (s, 6H, 2CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309265B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-2a97c086693349e1bb32236e71b45e2c
출처 메모uspto-grants-2016_04