Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251342생성일: 2026년 10월 26일
Sodium Hydroxide → 3-[5-amino-4-(4-methyl-benzoyl)-pyrazol-1-yl]-N-cyclopropyl-4-methyl-benzamide
https://huagongshe.com/reaction/251342
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | Aminomalononitrile p-toluenesulphonate | HCID 563049 | — |
| 반응물 | 3-amino-N-cyclopropyl-4-methylbenzamide | HCID 11983854 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl orthoformate | HCID 31214 | — |
| 생성물 | 3-[5-amino-4-(4-methyl-benzoyl)-pyrazol-1-yl]-N-cyclopropyl-4-methyl-benzamide | HCID 11164703 | 30% |
반응 단계
A mixture of 3-amino-N-cyclopropyl-4-methyl-benzamide 1 (380 mg, 2.0 mmol) in 2.0 mL of triethyl orthoformate was stirred at 120° C. in microwave for 20 minutes. The solvent was removed under reduced pressure. The residue was dissolved in 5 mL of acetic acid and then was added aminomalononitrile p-toluenesulfonate (506 mg, 2.0 mmol) and sodium acetate (164 mg, 2.0 mmol). The reaction mixture was stirred at room temperature overnight. The mixture was diluted with 20 mL of water and then its pH was adjusted to 8.0 by aqueous NaOH. The resulting mixture was extracted with EtOAc (3×50 mL). The combined organic layers were washed with water (10 mL) and brine (10 mL), dried over MgSO4, filtered and concentrated in vacuo evaporated. The residue was purified by silica gel column chromatography (10/1, methylene chloride:methanol) to give 3-(5-amino-4-cyano-imidazol-1-yl)-N-cyclopropyl-4-methyl-benzamide 3 as a colorless solid (170 mg, 30%). HPLC (4 minute gradient) tR=1.39 min; MS m/z 282 [M+H].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07863314B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-58d9bc116e3d41c3b7a02aebc0b2eda8 |
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| 출처 메모 | uspto-grants-2011_01 |
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