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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1075678생성일: 2026년 10월 27일

Triethylamine → HCID 178484369, 화합물

https://huagongshe.com/reaction/1075678

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물1-t-Butoxycarbonyl-3,3-dimethylthioureaHCID 45092025—
반응물5-Amino-3-(quinol-4-ylmethylene)-2-oxindoleHCID 54536702—
촉매Mercuric ChlorideHCID 24085—
용매DimethylformamideHCID 6228—
용매Trifluoroacetic acidHCID 6422—
생성물HCID 178484369HCID 17848436950%

반응 단계

To a solution of 5-amino-3-(4-quinolylmethylen) -2-oxindole (431 mg, 1.5 mmol) in DMF (100 ml) containing triethylamine (202 mg, 2 mmol) was added 1-t-butoxycarbonyl-3,3-dimethylthiourea (409 mg, 2 mmol) and HgCl2 (543 mg, 2 mmol). The mixture was stirred at room temperature for 1 h and then filtered on a pad of celite. The residue was washed with ethyl acetate, the organic layer washed several times with water, dried and evaporated to dryness. The residue was chromatographed on silica gel using as eluant ethyl acetate/cyclohexane 2:1. The above obtained BOC-derivative was taken up in trifluoroacetic acid (10 ml) and then stirred for 1 h at room temperature. Ethyl acetate was added, the organic layer washed with 1N sodium hydroxide and brine, dried and evaporated. The residue was chromatographed on a LoBar RP18 column with water as eluant to give pure title compound after freeze-drying. Yield 50% (268 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05905149
출처 데이터셋uspto-grants-1999_05
ORD IDord-40844b03e22c4d1bbb85c3fbe6bee499
출처 메모uspto-grants-1999_05