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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44501생성일: 2026년 10월 24일

Triethylamine → Methyl 3-amino-5-chloro-2-nitrobenzoate

https://huagongshe.com/ko/reaction/44501

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물3-Amino-5-chloro-2-nitrobenzoic acidHCID 10727479—
반응물2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate MethanaminiumHCID 86621144—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-amino-5-chloro-2-nitrobenzoateHCID 1216561964%

반응 단계

A mixture of 3-amino-5-chloro-2-nitrobenzoic acid (43.2 g) and HATU (2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate Methanaminium, commercially available) (76 g) in MeOH (81 mL), Et3N (83 mL) and THF (300 mL) was stirred at room temperature for 3 h. When TLC showed no starting material, the solvent was removed in-vacuo and the residue was then diluted with EtOAc (2 L). It was then washed with brine (1 L×3) and dried over anhydrous Na2SO4, filtered and concentrated in-vacuo. The residue was then purified by silica gel chromatography eluted with EtOAc:petroleum ether=1:8 to afford the desired product as a yellow solid (29.5 g, yield 64%). 1H NMR (300 MHz, CDCl3): δ ppm 3.90 (s, 3H, s), 5.85 (br s, 2H), 6.80 (d, 1H, J=2.4 Hz), 6.90 (d, 1H, J=2.4 Hz); LC-MS: m/e=231 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541411B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8b28922414d3416db20db88695315086
출처 메모uspto-grants-2013_09