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HRID 1865208作成日:2026年10月27日

Acetaldehyde → 6-((6,7-bis(methoxy)-4-quinolinyl)oxy)-N-ethyl-1-methyl-1H-indazol-3-amine

https://huagongshe.com/reaction/1865208

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物6-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-1-methyl-1H-indazol-3-amineHCID 44562290—
溶媒DichloromethaneHCID 6344—
生成物6-((6,7-bis(methoxy)-4-quinolinyl)oxy)-N-ethyl-1-methyl-1H-indazol-3-amineHCID 44562291—

反応手順

To a stirred solution of 6-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-1-methyl-1H-indazol-3-amine (Example 120, 140 mg, 0.40 mmol) in dry DCM (Aldrich, 4.0 mL) at RT were added acetaldehyde (Aldrich, 21.1 mg, 0.48 mmol) followed by NaHB(OAc)3 (Aldrich, 102 mg, 0.48 mmol). After being stirred for 4 h at RT, the reaction was quenched by addition of water. The aqueous layer was extracted with DCM. The organic layer was dried with MgSO4, filtered and concentrated in vacuo. Purification by silica gel chromatography (DCM/acetone: 100/0 to 60/40) afforded the title compound. MS (ESI, pos. ion) m/z: 379.3 (M+1). Mass Calc'd for C21H22N4O3: 378.43.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07626030B2
出典データセットuspto-grants-2009_12
ORD IDord-3bfd345eb81840b485ef73f474b63ded
出典メモuspto-grants-2009_12