関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | Ethyl 2-formyl-3-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate | HCID 22574402 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 178469552 | HCID 178469552 | 59.5% |
反応手順
A suspension of ethyl 2-formyl-3-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate (Preparation 3)(1.50 g, 5.66 mmol) in 1:1 CH2Cl2:MeOH (15 mL) was chilled in an ice bath before the addition of sodium borohydride (0.214 g, 5.66 mmol). The reaction was stirred at 0° C. for one hour and then quenched by the addition of water (30 mL). While continuing to chill in an ice bath, the mixture was adjusted to pH 4 by the careful addition of 1 N HCl. The resulting thick mixture was stirred at 0° C. for one hour before filtering. The collected solid was washed with water and dried in vacuo, affording the title compound (0.90 g) as an off-white solid. The filtrate was concentrated in vacuo to a volume of about 50 mL, more water was added, and the mixture was again filtered after chilling in ice, giving an additional 0.29 g of the title product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06852731B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-06d3f9e9c7164959ace2f8f6c2c9e567 |
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| 出典メモ | uspto-grants-2005_02 |
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