Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diisopropylethylamine → N-[2-(1,3-dimethylbutyl)phenyl]-2-iodothiophene-3-carboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | PyBroP | HCID 2733179 | — |
| 반응물 | 2-(1,3-Dimethylbutyl)aniline | HCID 11528441 | — |
| 반응물 | 2-Iodothiophene-3-carboxylic acid | HCID 23094022 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-[2-(1,3-dimethylbutyl)phenyl]-2-iodothiophene-3-carboxamide | HCID 11315926 | 21.3% |
반응 단계
Under protective gas (argon), 0.56 ml (3.38 mmol) of N,N-diisopropylethylamine and 1.18 g (2.5 mmol) of bromotrispyrrolidinophosphonium hexafluorophosphate (PyBrop) are added to a solution of 516 mg (2.0 mmol) of 2-iodothiophene-3-carboxylic acid and 300 mg (1.7 mmol) of 2-(1,3-dimethylbutyl)phenylamine in 10 ml of acetonitrile. The reaction mixture is stirred at room temperature for 24 hours and, for work-up, added to water, extracted with ethyl acetate, dried over sodium sulphate and concentrated under reduced pressure. Column chromatography (cyclohexane/ethyl acetate gradient) gives 150 mg (21% of theory) of N-[2-(1,3-dimethylbutyl)phenyl]-2-iodothiophene-3-carboxamide [log P (pH 2.3)=4.14].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07745483B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-700d18bc9c354bc19c34272aa8316f70 |
| 출처 메모 | uspto-grants-2010_06 |