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HRID 1445062作成日:2026年10月26日

3-Fluorobenzyl chloride → 1-(3-fluorobenzyl)-2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine hydrochloride

https://huagongshe.com/reaction/1445062

反応式

関与物質

役割名称HCID仕込み量
反応物3-Fluorobenzyl chlorideHCID 9974—
反応物18-Crown-6HCID 28557—
反応物Potassium tert-butoxideHCID 23665647—
反応物2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridineHCID 67141589—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3-fluorobenzyl)-2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine hydrochlorideHCID 6714286010%

反応手順

18-Crown-6 (2.5 mg, 0.0097 mmol) and potassium tert-butoxide (33 mg, 0.291 mmol) were added to a solution of 2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine (24 mg, 0.097 mmol) prepared in Example 242 in anhydrous tetrahydrofuran (0.5 ml). The reaction mixture was stirred for 30 minutes at room temperature and 3-fluorobenzyl chloride (20 μl, 0.16 mmol) was added thereto. The reaction mixture was stirred overnight and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography. The resulting product was dissolved in ethyl acetate, saturated with hydrochloric acid gas, and then filtered to give 3.8 mg of the titled compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07662832B2
出典データセットuspto-grants-2010_02
ORD IDord-95ea7496bed34927bef4b3cdc34fb111
出典メモuspto-grants-2010_02