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HRID 1922765作成日:2026年10月27日

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

https://huagongshe.com/reaction/1922765

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-2-iodoethaneHCID 136438—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物5-(2-Ethylbenzoimidazol-1-yl)-7-morpholin-4-ylthiazolo[5,4-d]pyrimidineHCID 59605632—
溶媒TetrahydrofuranHCID 8028—
生成物5-(2-Ethylbenzoimidazol-1-yl)-2-iodo-7-morpholin-4-ylthiazolo[5,4-d]pyrimidineHCID 59606186—

反応条件

温度-5 °C

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173650B2
出典データセットuspto-grants-2012_05
ORD IDord-2995dab65c564bfe9440a6e3e763c92e
出典メモuspto-grants-2012_05