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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264325생성일: 2026년 10월 25일

Hydrochloric Acid → 2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-2-[(2-methyl-5-tetrazolyl)methyl]acetic acid

https://huagongshe.com/reaction/264325

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물Methyl 2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-2-[(2-methyl-5-tetrazolyl)methyl]acetateHCID 22856288—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-2-[(2-methyl-5-tetrazolyl)methyl]acetic acidHCID 2285628298%

반응 단계

Methyl 2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-2-[(2-methyl-5-tetrazolyl)methyl]acetate (1.0 g, 2.27 mmol) is dissolved in tetrahydrofuran (11.3 mL) and water (11.3 mL). To this solution is added lithium hydroxide hydrate (0.095 g, 2.27 mmol), and the reaction is stirred at room temperature for 2 hours. The reaction is then acidified to pH=~3 using 1N hydrochloric acid, and extracted well with ethyl acetate. The combined organic extracts are washed with brine, dried (Na2SO4), and the solvent is evaporated to provide 2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-2-[(2-methyl-5-tetrazolyl)methyl]acetic acid (0.96 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646167
출처 데이터셋uspto-grants-1997_07
ORD IDord-25eb088b0ca34bc2848c7bfe59f586a5
출처 메모uspto-grants-1997_07