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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1922848생성일: 2026년 10월 26일

Triethylamine → Acetic acid 1,1-dimethyl-2-{3-[9-methyl-2-(2-methylbenzoimidazol-1-yl)-6-morpholin-4-yl-9H-purin-8-ylmethyl]azetidin-1-yl}-2-oxoethyl ester

https://huagongshe.com/reaction/1922848

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Acetoxyisobutyroyl chlorideHCID 123496—
반응물8-Azetidin-3-ylmethyl-2-(2-isopropylbenzoimidazol-1-yl)-9-methyl-6-morpholin-4-yl-9H-purineHCID 59605635—
용매TetrahydrofuranHCID 8028—
생성물Acetic acid 1,1-dimethyl-2-{3-[9-methyl-2-(2-methylbenzoimidazol-1-yl)-6-morpholin-4-yl-9H-purin-8-ylmethyl]azetidin-1-yl}-2-oxoethyl esterHCID 5960602880.7%

반응 단계

A mixture of 8-azetidin-3-ylmethyl-2-(2-isopropylbenzoimidazol-1-yl)-9-methyl-6-morpholin-4-yl-9H-purine (100 mg, 0.22 mmol), acetic acid 1-chlorocarbonyl-1-methylethyl ester (32 μL, 0.22 mmol) and NEt3 (29 μL, 0.22 mmol) in THF (3 mL) was allowed to stir at r.t. for 16 h then concentrated in vacuo. The resulting residue was partitioned between DCM and H2O, the organic phase dried (Na2SO4) and concentrated in vacuo. The residue was purified by column chromatography (Si—PCC, MeOH:EtOAc, 0-7%) affording the title compound as a white foam (97 mg, 75%)._LCMS (method A): RT 2.65 min [M+H]+ 575.3

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173650B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-ab8351f3031343d0a6613bb8f88faf6e
출처 메모uspto-grants-2012_05