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HRID 8930作成日:2026年10月23日

Piperidine → (1H-Benzimidazol-2-ylmethyl)-(4-piperidin-1-ylmethyl-benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine

https://huagongshe.com/ja/reaction/8930

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物4-{[(1H-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehydeHCID 21984982—
溶媒MethanolHCID 887—
生成物(1H-Benzimidazol-2-ylmethyl)-(4-piperidin-1-ylmethyl-benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amineHCID 2198509230%

反応手順

Using General Procedure A: To a stirred solution of 4-{[(1H-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (AMD9882) (144 mg, 0.36 mmol) in dry MeOH (5 mL) was added piperidine (0.040 mL, 0.40 mmol) and sodium cyanoborohydride (44 mg, 0.70 mmol) and the mixture stirred for 5 h. Purification of the crude product by radial chromatography on silica gel (1 mm plate, CH2Cl2/MeOH/NH4OH, 50:1:1) afforded the desired adduct (50 mg, 30%) as a white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091217B2
出典データセットuspto-grants-2006_08
ORD IDord-16bde70fcd064c18a0e2fb70f4c85ac0
出典メモuspto-grants-2006_08