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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56555생성일: 2026년 10월 24일

Methanamine, N-methoxy-, hydrochloride (1:1) → N,2-dimethoxy-N-methyl-2-(4-(2-methyl-2H-tetrazol-5-yl)phenyl)acetamide

https://huagongshe.com/ko/reaction/56555

반응식

참여 물질

역할이름HCID투입량
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
반응물2-methoxy-2-(4-(2-methyl-2H-tetrazol-5-yl)phenyl)acetic acidHCID 58431999—
용매DichloromethaneHCID 6344—
생성물N,2-dimethoxy-N-methyl-2-(4-(2-methyl-2H-tetrazol-5-yl)phenyl)acetamideHCID 5843208742%

반응 단계

To a solution of 2-methoxy-2-(4-(2-methyl-2H-tetrazol-5-yl)phenyl)acetic acid (0.87 g, 3.5 mmol) in anhydr CH2Cl2 (10 ml) was added N,N-diisopropylethylamine (1.36 g, 10.5 mmol) while cooling over an ice bath. bis(2-Methoxyethyl)aminosulfur trifluoride (0.93 g, 4.2 mmol) was added and stirred 15 min. N,O-Dimethylhydroxylamine HCl (0.512 g, 5.25 mmol) was added and the mixture was allowed to stir overnight while warming to room temp. Saturated aqueous NaHCO3 (15 ml) was added and stirred for 5 min. The organic layer was dried over Na2SO4 and evaporated to dryness. Purification by chromatography (60% EtOAc-hexanes) gave N,2-dimethoxy-N-methyl-2-(4-(2-methyl-2H-tetrazol-5-yl)phenyl)acetamide as a clear oil (0.425 g, 42% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434707B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ffc7825c7ae34153b58a106308aed439
출처 메모uspto-grants-2016_09