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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1464800생성일: 2026년 10월 24일

Triethylamine → 6-[5-(2-Oxo-Hexahydro-Thieno[3,4-D]Imidazol-4-Yl)-Pentanoylamino]-Hexanoic Acid

https://huagongshe.com/ko/reaction/1464800

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6-[5-(2-Oxo-Hexahydro-Thieno[3,4-D]Imidazol-4-Yl)-Pentanoylamino]-Hexanoic AcidHCID 446905—
반응물Methyl 6-aminohexanoate hydrochlorideHCID 11499324—
반응물7-Amino-4-chloro-3-[(2-phenyl)ethoxy]-1H-2-benzopyran-1-oneHCID 13654068—
용매WaterHCID 962—
용매Thionyl ChlorideHCID 24386—
생성물6-[5-(2-Oxo-Hexahydro-Thieno[3,4-D]Imidazol-4-Yl)-Pentanoylamino]-Hexanoic AcidHCID 446905—
생성물HCID 54466620HCID 54466620—

반응 단계

6-(Biotinylamino)caproic acid was prepared from N-hydroxysuccinimido biotinate (Jasiewicz et al., Exp. Cell Res. 100, pp 213-217 (1976)) and 6-aminocaproic acid methyl ester hydrochloride by a previously described method (Hofmann et al., Biochemistry 23, pp 2547-2553 (1984)). 6-(Biotinylamino)caproic acid chloride was prepared by incubating 6-(biotinylamino)caproic acid (0.36 g, 1 mmole) in 4 ml of thionyl chloride at 25°-35° C. for 1 h, and excess thionyl chloride was removed under reduced pressure. The residue was dissolved in DMF and 7-amino-4-chloro-3-(2-phenylethoxy)isocoumarin (0.34 g, 1 mmole) and Et3N (0.1 g, 1 mmole) were added and the reaction mixture was stirred at r.t. overnight. The product was purified from column chromatography and eluted with CH2Cl2 :MeOH=10:1, yield, 28%, mp 163°-167° C., NMR was consistent with the assigned structure, mass spectra (FAB+) m/e=655 (M+1). Anal. Calc. for C33H39N4O6ClS.H2O: C, 58.87; H, 6.14; N, 8.32; Cl, 5.27. Found: C, 58.72; H, 6.22; N, 8.90; Cl, 5.50.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05306824
출처 데이터셋uspto-grants-1994_04
ORD IDord-60709878962445688bdd6e068784e906
출처 메모uspto-grants-1994_04