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HRID 51537作成日:2026年10月25日

Acetic Acid → HCID 178480946、化合物

https://huagongshe.com/reaction/51537

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Trimethyl orthoformateHCID 9005—
反応物1-MethylpiperazineHCID 53167—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物4-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyrimidin-7-yl)-cyclohexanoneHCID 22736413—
溶媒1,1-DichloroethaneHCID 6365—
生成物HCID 178480946HCID 17848094624.8%

反応手順

A mixture of 4-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-cyclohexanone (5.6 g, 14.9 mmol), N-methylpiperazine (3.3 mL, 29.8 mmol), acetic acid (2.6 mL, 44.7 mmol), and trimethylorthoformate (9.9 mL, 89.4 mmol) in dichloroethane (100 mL) was stirred at ambient temperature under an atmosphere of nitrogen for 1 hr. Sodium triacetoxyborohydride (14.2 g, 67.05 mmol) was added into the mixture and stirred at ambient temperature under an atmosphere of nitrogen for 18 hours. The solvent was removed under reduced pressure. The residue was partitioned between saturated aqueous sodium bicarbonate solution and ethyl acetate. The water phase was further extracted with ethyl acetate and the combined organic extracts were dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash chromatography on silica gel using triethylamine/dichloromethane (2:98) followed by methanol/triethylamine/dichloromethane (2:3:95) as mobile phase to yield trans-4-chloro-5-iodo-7-[4-(4-methylpiperazino)cyclohexyl]-7H-pyrrolo[2,3-d]pyrimidine (1.7 g, 3.7 mmol). 1H NMR (DMSO-d6, 400 MHz) 8.63 (s, 1H), 8.12 (s, 1H), 4.63 (br, 1H), 2.15 (s, 3H), 1.94 (br, 6H), 1.45 (br, 2H) RP-20 HPLC (Hypersil C18, 5 μm, 250×4.6 mm; 25%-100% over 15 min with 0.05 M ammonium acetate, 1 mL/min) Rt 6.17 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713474B2
出典データセットuspto-grants-2004_03
ORD IDord-77b7e1c130ff4c6882060a79fb95c1e7
出典メモuspto-grants-2004_03