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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54856생성일: 2026년 10월 23일

Triethylamine → HCID 178439611, 화합물

https://huagongshe.com/ko/reaction/54856

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PentafluorophenolHCID 13041—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물2-adamantyloxycarbonyl-alpha-methyl-DL-tryptophanHCID 14802503—
반응물HCID 178478691HCID 178478691—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물HCID 178439611HCID 17843961147.3%

반응 단계

To a solution of 2-adamantyloxycarbonyl-α-methyl-DL-tryptophan (0.401 g, 1.01 mmol) in dry ethyl acetate (6 mL) and N,N-dimethylformamide (4 mL) under nitrogen atmosphere was added pentafluorophenol (0.189 g, 1.03 mmol) followed by 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (0.200 g, 1.04 mmol). This mixture was stirred 2 hours, then triethylamine (0.36 mL, 2.6 mmol) and histamine dihydrochloride (0.240 g, 1.30 mmol) were added. After stirring an additional 40 hours, the resulting mixture was diluted with ethyl acetate (20 mL), and washed with water. The organic phase was dried over MgSO4, concentrated, purified by flash chromatography (SiO2, 4×20 cm, 230-400 mesh, 10% methanol/dichloromethane eluant), and dried for 48 hours under vacuum at 70° C. to provide 0.234 g (47%) of product; 1H NMR (CDCl3) δ1.40-1.60 (2H, m), 1.57 (3H, s), 1.65-2.00 (13H, m), 2.65-2.75 (2H, m), 3.25-3.45 (4H, m), 4.82 (1H, br s), 5.42 ([H, br s), 6.67 (1H, s), 6.81 (1H, br s), 6.91 (1H, br s),7.00-7.20 (2H, m), 7.34 (1H, d, J 7 Hz), 7.46 (1H, s), 7.55 (1H, d, J 7 Hz), 8.67 (1H, br s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622983
출처 데이터셋uspto-grants-1997_04
ORD IDord-85cef224fcff45b1b389493bd1530816
출처 메모uspto-grants-1997_04