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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62723생성일: 2026년 10월 24일

Hydrochloric Acid → HCID 67041575, 화합물

https://huagongshe.com/ko/reaction/62723

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylethylamineHCID 81531—
반응물3,5-Dichloro-4-ethoxybenzoic acidHCID 820138—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물HCID 86666595HCID 86666595—
용매DimethylformamideHCID 6228—
생성물HCID 67041575HCID 6704157557.7%

반응 단계

A solution of 3,5-dichloro-4-ethoxybenzoic acid (1) (285 mg, 1.21 mmol) and DIPEA (1.05 mL, 6.05 mmol) in DMF (2.5 mL) was added to HATU (690 mg, 1.82 mmol) and the orange mixture was stirred for 5 min prior to the addition of methyl 4-amino-2-methylbenzoate (2) (200 mg, 1.21 mmol) in DMF (1 mL). The resulting dark orange solution was stirred overnight for 18 h. 2 M HCl (10 mL) was added and stirring continued for 10 min, and then the mixture was extracted with diethyl ether. The organic layer was washed with water (3×15 mL), dried over MgSO4, filtered and the solvent was evaporated in vacuo. The yellow residue was purified by silica gel chromatography (40 g, 0-100% EtOAc in isohexane) to afford methyl 4-(3,5-dichloro-4-ethoxybenzamido)-2-methylbenzoate (3) (267 mg, 56%): m/z 380 (M−H)− (ES−). 1H NMR (400 MHz, CDCl3) δ: 7.97 (1H, s), 7.80 (3H, m), 7.54 (1H, dd), 7.51 (1H, d), 4.18 (2H, q), 3.89 (3H, s), 2.63 (3H, s), 1.49 (3H, t).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447028B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-632a4c8a5af245d3bd79e7bb8d9e8145
출처 메모uspto-grants-2016_09