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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10991생성일: 2026년 10월 25일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → benzyl N-[(6S,8R)-4-oxo-6-[[4-(N-phenylmethoxycarbonylcarbamimidoyl)phenyl]methylcarbamoyl]-8-prop-2-enyl-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidin-3-yl]-N-prop-2-enylcarbamate

https://huagongshe.com/reaction/10991

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물HOAtHCID 181649—
반응물Sodium BicarbonateHCID 516892—
반응물(6S,8R)-8-allyl-3-(allyl-benzyloxycarbonyl-amino)-4-oxo-4,6,7,8-tetrahydro-pyrrolo[1,2-a]pyrimidine-6-carboxylic AcidHCID 57444828—
반응물Benzyl ((4-(aminomethyl)phenyl)(imino)methyl)carbamate hydrochlorideHCID 145832047—
용매Ethyl AcetateHCID 8857—
용매dichloromethane N,N-dimethylformamideHCID 22350042—
생성물benzyl N-[(6S,8R)-4-oxo-6-[[4-(N-phenylmethoxycarbonylcarbamimidoyl)phenyl]methylcarbamoyl]-8-prop-2-enyl-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidin-3-yl]-N-prop-2-enylcarbamateHCID 14585721920.8%

반응 단계

To a solution of 28d (172 mg, 0.420 mmol) and [(4-aminomethyl-phenyl)-imino-methyl]-carbamic acid benzyl ester hydrochloride (180 mg, 0.504 mmol) in 3.6 mL CH2Cl2/DMF (5:1) at 0° C., was added HOAT (113 mg, 0.588 mmol), NaHCO3 (141 mg, 1.68 mmol), and EDCI (113 mg, 0.588 mmol). The mixture was allowed to warm to rt and stir for 64 h. The reaction was diluted with EtOAc and the organic phase was washed with H2O, 1N HCl, H2O, and brine. The organic phase was dried (Na2SO4) and concentrated. The residue obtained was purified by flash chromatography (75% EtOAc/hexanes) to afford 59 mg of intermediate 28e.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094783B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-384eab5d229c455fb8dd63aeadcf8621
출처 메모uspto-grants-2006_08