戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 11754作成日:2026年10月24日

N-(3,4-dimethoxybenzyl)-7-(2-fluorobenzyl)4-(2-furyl)-7H-pyrrolo[2,3-d]pyrimidine-2-amine → 7-(2-fluorobenzyl)-4-(2-furyl)-7H-pyrrolo[2,3-d]pyrimidine-2-amine

https://huagongshe.com/ja/reaction/11754

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3,4-dimethoxybenzyl)-7-(2-fluorobenzyl)4-(2-furyl)-7H-pyrrolo[2,3-d]pyrimidine-2-amineHCID 21976416—
溶媒Trifluoroacetic acidHCID 6422—
生成物7-(2-fluorobenzyl)-4-(2-furyl)-7H-pyrrolo[2,3-d]pyrimidine-2-amineHCID 990468851.4%

反応手順

A solution of N-(3,4-dimethoxybenzyl)-7-(2-fluorobenzyl)4-(2-furyl)-7H-pyrrolo[2,3-d]pyrimidine-2-amine (110 mg, 0.24 mmol) in TFA (1 mL) was heated to 50° C. for 3 h, concentrated in vacuo, treated with saturated NaHCO3, extracted with EtOAc, dried (MgSO4), concentrated in vacuo, purified by chromatography (EtOAc:Heptane, 1:4) and recrystallised (EtOAc) to give the title compound (38 mg, 51%) as a cream solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098333B2
出典データセットuspto-grants-2006_08
ORD IDord-33bf0de3f8aa48d1816747caea2ecde9
出典メモuspto-grants-2006_08