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HRID 6919作成日:2026年10月23日

Formaldehyde → [4-Benzyl-5-(3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-4H-[1,2,4]triazol-3-ylmethyl]-(2-methoxy-ethyl)-methyl-amine

https://huagongshe.com/ja/reaction/6919

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物[4-Benzyl-5-(3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-4H-[1,2,4]triazol-3-ylmethyl]-(2-methoxy-ethyl)-amineHCID 10409077—
溶媒DichloromethaneHCID 6344—
生成物[4-Benzyl-5-(3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-4H-[1,2,4]triazol-3-ylmethyl]-(2-methoxy-ethyl)-methyl-amineHCID 10432290—

反応手順

The amine from example 43 (50 mg, 0.12 mmol), formaldehyde (37% aq, 40 μl, 0.49 mmol) and sodium triacetoxyborohydride (51 mg, 0.24 mmol) in dichloromethane (1 ml) was stirred vigorously at room temperature for 21 hours. The reaction mixture was partitioned between dichloromethane and aqueous sodium carbonate solution, and the layers separated. The organic phase was dried (MgSO4), evaporated under reduced pressure, and the product triturated from ether to afford the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084145B2
出典データセットuspto-grants-2006_08
ORD IDord-6f19733c657e4b04b7ed2ac578424390
出典メモuspto-grants-2006_08