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HRID 7142作成日:2026年10月23日

Sodium triacetoxyborohydride → N-(5-butyl-2-pyridinylmethyl)-N'-(1H-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine

https://huagongshe.com/ja/reaction/7142

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物5-n-Butylpyridine-2-carboxaldehydeHCID 21396266—
反応物N-[(1H-Benzo[d]imidazol-2-yl)methyl]-N-(4-(aminomethyl)-benzyl)-5,6,7,8-tetrahydroquinolin-8-amineHCID 21985008—
溶媒DichloromethaneHCID 6344—
生成物N-(5-butyl-2-pyridinylmethyl)-N'-(1H-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamineHCID 22018809—

反応手順

Using general procedure B: N-(1H-benzimidazol-2-ylmethyl)-N-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine (0.1258 g, 0.316 mmol) and 5-n-butylpyridine-2-carboxaldehyde (0.0603 g, 0.294 mmol) were reacted with NaBH(OAc)3 (0.0942 g, 0.444 mmol) in CH2Cl2 (2.5 mL). Purification of the crude material by radial chromatography (2 mm TLC plate, 50:1:1 CH2Cl2: CH3OH: NH4OH) provided 0.0713 g (45%) of AMD9398 (free base).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084155B2
出典データセットuspto-grants-2006_08
ORD IDord-b8796c8cf3334b43b0cdd5ad9d83bed5
出典メモuspto-grants-2006_08