関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Chlorine | HCID 24526 | — |
| 反応物 | 2-Bromoisonicotinic acid | HCID 222701 | — |
| 反応物 | Aluminum(III) Chloride | HCID 6451240 | — |
| 反応物 | 4-Methyl-3H-benzooxazol-2-one | HCID 12709336 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 6-(2-bromo-pyridine-4-carbonyl)-4-methyl-3H-benzoxazol-2-one | HCID 58181213 | — |
反応手順
2.20 mL (30.0 mmol) thionyl chloride and 0.390 mL (4.80 mmol) DMF were added to 2.00 g (9.90 mmol) 2-bromopyridine-4-carboxylic acid in 30 mL DCM and refluxed for 2 h. The reaction mixture was evaporated to dryness and coevaporated twice with toluene. The residue was combined with 6.24 g (46.8 mmol) aluminium trichloride and 1.50 g (10.1 mmol) 4-methyl-3H-benzoxazol-2-one and the mixture obtained was stirred overnight at 110° C. and for 5 hours at 130° C. The mixture was decomposed with ice water and extracted twice with DCM. The organic phases were dried on magnesium sulphate, filtered and evaporated down i. vac. The residue was triturated with DIPE/MeOH and suction filtered. The product obtained is a mixture of the corresponding bromine and chlorine compound (40/60).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08629137B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-a7869bb0c12f4d85aef225774e98f332 |
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| 出典メモ | uspto-grants-2014_01 |
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