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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16974생성일: 2026년 10월 24일

Hydrochloric Acid → ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetate

https://huagongshe.com/ko/reaction/16974

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물tert-ButanolHCID 6386—
반응물TriethylamineHCID 8471—
반응물Glycine ethyl esterHCID 12176—
반응물Chlorosulfonyl isocyanateHCID 70918—
용매DichloromethaneHCID 6344—
생성물ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetateHCID 1844991485%

반응 단계

To a stirred solution of chlorosulfonyl isocyanate (1.43 g, 10.0 mmol) in CH2Cl2 (20 mL) at 0° C. was added 2-methyl-propan-2-ol (0.74 g, 10.0 mmol) at such a rate that the reaction solution temperature did not rise above 5° C. After being stirred for 1.5 h, a solution of glycine ethyl ester (1.45 g, 12.0 mmol) and Et3N (3.2 mL, 25.0 mmol) in CH2Cl2 (20 mL) was added at such a rate that the reaction temperature didn't rise above 5° C. When the addition was completed, the solution was warmed to RT and stirred overnight. The reaction mixture was poured into 10% HCl and extracted with CH2Cl2. The organic layer was washed with saturated NaCl, dried (Mg2SO4) and filtered. After removal of the solvent, the crude product was washed with CH2Cl2 to afford ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetate (2.4 g, 85%). 1H-NMR (DMSO): δ 10.85 (s, 1H), 8.04 (t, J=6.0 Hz, 1H), 4.07 (q, J=5.6 Hz, 2H), 3.77 (d, J=6.0 Hz, 2H), 1.40 (s, 9H), 1.18 (t, J=7.2 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737283B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a3e6e6c72fdd44fab0a361edc472f42e
출처 메모uspto-grants-2010_06