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HRID 1601027作成日:2026年10月27日
Sodium triacetoxyborohydride → 7-Bromo-2-(1-(4-cyanobenzyl)-5-imidazolylmethyl)-1,2,3,4-tetrahydroisoquinoline
https://huagongshe.com/reaction/1601027
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | 4-[(5-Formylimidazol-1-yl)methyl]benzonitrile | HCID 10632289 | — |
| 反応物 | 7-Bromo-1,2,3,4-tetrahydroisoquinoline | HCID 10729255 | — |
| 溶媒 | 1,1,2,2-Tetrachloroethane | HCID 6591 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 7-Bromo-2-(1-(4-cyanobenzyl)-5-imidazolylmethyl)-1,2,3,4-tetrahydroisoquinoline | HCID 9866080 | — |
反応手順
To a solution of 7-bromo-1,2,3,4-tetrahydroisoquinoline (0.742 g, 3.5 mmol) in CHCl2CHCl2 (15 mL) was added 1-(4-cyanobenzyl)-5-imidazole carboxaldehyde (0.812 g, 3.85 mmol), 4 Å sieves and NaBH(OAc)3 (1.11 g, 5.25 mmol). The mixture was stirred at room temperature for 16 h. and a further portion of NaBH(OAc)3 (0.55 g, 2.6 mmol) was added. After an additional 24 h the mixture was diluted with EtOAc, filtered through celite, washed with brine, dried (Na2SO4) and concentrated. The residue was stirred in 2N Hcl (50 mL) for 2 h. then extracted with ether. The aqueous layer was basified with 6N KOH and extracted 3× CH2Cl2 which was then washed with brine, dried (Na2SO4) and the solvent evaporated in vacuo. Crystallization from ether afforded the title compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05977134 |
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| 出典データセット | uspto-grants-1999_11 |
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| ORD ID | ord-7b67745e3ea741c88889f1d8462fafc0 |
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| 出典メモ | uspto-grants-1999_11 |
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