Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12829생성일: 2026년 10월 23일
2-Aminoadamantane hydrochloride → 2'-methyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acid adamantan-2-ylamide
https://huagongshe.com/ko/reaction/12829
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Aminoadamantane hydrochloride | HCID 25331 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborate | HCID 9857522 | — |
| 반응물 | 2'-methyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acid | HCID 58972849 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2'-methyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acid adamantan-2-ylamide | HCID 25013541 | 77% |
반응 단계
2′-Methyl-2′H-[1,3′]bipyrazolyl-4′-carboxylic acid (Intermediate 8, 50 mg, 0.26 mmol) was dissolved in a mixture of dry dichloromethane (3.2 mL) and dry DMF (0.8 mL). DIPEA (0.23 mL, 1.3 mmol) and TSTU (93 mg, 0.28 mmol) were added to the above mixture. After the mixture was stirred for 1 h, the appearance of active ester was detected by LC-MS. Then 2-aminoadamantane hydrochloride (58 mg, 0.31 mmol) was added. After another 2 hours water was added and the organic layer was separated. The aqueous layer was extracted twice with dichloromethane. The combined organic phases were dried under vacuum and purified by C-18 reversed phase prep-HPLC with a gradient of 10-100% acetonitrile/water to give 2′-methyl-2′H-[1,3′]bipyrazolyl-4′-carboxylic acid adamantan-2-ylamide (65 mg, 77%). Mass spectrum: m/z: 362.2 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728029B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-e39314f40e6043cb9d02def678859e3f |
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| 출처 메모 | uspto-grants-2010_06 |
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