関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | p-Acetamidobenzoic acid | HCID 19266 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | 5-Amino-2-(naphthalen-1-ylamino)thiazole-4-carboxamide | HCID 86703368 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(4-Acetamidobenzamido)-2-(naphthalen-1-ylamino)thiazole-4-carboxamide | HCID 72550189 | 29.2% |
反応手順
To a mixture of 4-acetamidobenzoic acid (0.151 g, 0.845 mmol) and a catalytic amount of DMF in dry THF (8 mL) was added dropwise oxalyl chloride (0.12 mL, 1.40 mmol) at 0° C., and the mixture was stirred for 2 hrs at rt. The solvent was evaporated, and the residual oxalyl chloride was removed with azeotropic distillation using toluene under nitrogen atmosphere. The resulting acid chloride was then dissolved in pyridine (5 mL) and cooled to 0° C. To this solution, a solution of 5-amino-2-(naphthalene-1-ylamino)thiazole-4-carboxamide (0.2 g, 0.70 mmol) in pyridine (5 mL) was added at 0° C., and the mixture was stirred for 12 hrs at rt. The solvent was evaporated, and the residue was suspended into I M HCl, and the resulting solids were collected and dried. The crude solids were purified by silica gel column chromatography eluted with 3% MeOH in DCM to give 91 mg (29% yield) of the titled compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09102637B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-c9bdf21784cd4ffaae4e32a4c4f29af4 |
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| 出典メモ | uspto-grants-2015_08 |
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