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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1922765생성일: 2026년 10월 26일

1-Chloro-2-iodoethane → 5-(2-Ethylbenzoimidazol-1-yl)-2-iodo-7-morpholin-4-ylthiazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/1922765

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-2-iodoethaneHCID 136438—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물5-(2-Ethylbenzoimidazol-1-yl)-7-morpholin-4-ylthiazolo[5,4-d]pyrimidineHCID 59605632—
용매TetrahydrofuranHCID 8028—
생성물5-(2-Ethylbenzoimidazol-1-yl)-2-iodo-7-morpholin-4-ylthiazolo[5,4-d]pyrimidineHCID 59606186—

반응 조건

온도-5 °C

반응 단계

A solution of 5 -(2-ethylbenzoimidazol-1-yl)-7-morpholin-4-ylthiazolo[5,4-d]pyrimidine (1.92 g, 5.23 mmol) in THF (60 mL) was cooled to −40° C. before the drop wise addition of LiHMDS (6.3 mL, 6.28 mmol, 1 M solution in THF). The resulting mixture was warmed to −5° C. over 30 min then mixture was cooled back to −30° C. before the addition of a solution of 1-chloro-2-iodoethane (2.0 g, 10.47 mmol) in THF (6 mL) The resulting mixture was allowed to warm to 0° C. then quenched with NH4Cl and extracted with EtOAc. The combined organics were washed with brine then dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, EtOAc:DCM, 50-80%) followed by recrystallisation from iPrOAc affording the title compound as a yellow solid (1.58 g, 62%)._LCMS (method A): RT 3.50 min [M+H]+ 493.0

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173650B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-2995dab65c564bfe9440a6e3e763c92e
출처 메모uspto-grants-2012_05