Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1011903생성일: 2026년 10월 26일
Dicyclohexylcarbodiimide → [5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-[4-(2-hydroxy-ethyl)-[1,4]diazepan-1-yl]-methanone
https://huagongshe.com/reaction/1011903
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | 2-(1,4-Diazepan-1-yl)ethan-1-ol | HCID 2736550 | — |
| 반응물 | 5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazole-3-carboxylic acid | HCID 67314297 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | [5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-[4-(2-hydroxy-ethyl)-[1,4]diazepan-1-yl]-methanone | HCID 67314874 | 40% |
반응 단계
To a suspension of 0.060 g (0.18 mmol) of 5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazole-3-carboxylic acid in 2 ml of CH2Cl2 was added 0.031 g (0.22 mmol) of 2-(1,4-diazepan-1-yl)ethan-1-ol, diluted in 1.7 ml of CH2Cl2. This solution was treated at 0° C. with 0.048 g (0.23 mmol) of DCC. The reaction was allowed to warm up over night to RT, then partitioned between aqueous saturated NaHCO3/EtOAc (3×). The organic phases were washed with aqueous saturated NaHCO3, dried (Na2SO4) and evaporated. The residue was suspended in EtOAc and filtered to remove the DCC urea. Purification by flash chromatography (SiO2—NH2, n-heptane/EtOAc 1:4) gave 0.033 g (39%) of [5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-[4-(2-hydroxy-ethyl)-[1,4]diazepan-1-yl]-methanone as white oil. MS: 459.3 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07977358B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-e741a131714d448195f6d2f35319d480 |
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| 출처 메모 | uspto-grants-2011_07 |
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