참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzamide, N-(4-fluoro-3-nitrophenyl)-N-methyl- | HCID 11460004 | — |
| 반응물 | 3-Aminopropanamide hydrochloride | HCID 22222288 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-[4-(2-carbamoyl-ethylamino)-3-nitro-phenyl]-N-methyl-benzamide | HCID 21884188 | — |
반응 단계
N-(4-fluoro-3-nitro-phenyl)-N-methyl-benzamide (1.47 g, 5.37 mmol) was taken up in dry acetonitrile under argon, DIEA (2.08 g, 16.11 mmol, 2.80 ml) and β-alanine amide hydrochloride (1.00 g, 8.06 mmol) were added. The reaction mixture was heated to 80° C. for 48 h. The reaction was poured into 1N HCl and the aqueous layer was extracted 3× with ethyl acetate. The combined organic layers were washed with water, brine and dried over magnesium sulfate. The solution was filtered and the solvent removed under reduced pressure. The residue was triturated twice with cold hexane and dried to give N-[4-(2-carbamoyl-ethylamino)-3-nitro-phenyl]-N-methyl-benzamide. (1.75 g, 95%)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07138420B2 |
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| 출처 데이터셋 | uspto-grants-2006_11 |
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| ORD ID | ord-e834417c845e47c1acbbc78398a6df70 |
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| 출처 메모 | uspto-grants-2006_11 |
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