참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lysergic Acid | HCID 6717 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | Ethyl N-ethyl-beta-alaninate | HCID 90223 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Lysergic Acid N-ethyl N-(2-carbethoxy)ethyl Amide | HCID 66871214 | — |
반응 단계
A mixture of lysergic acid 5 (934 mg, 3.27 mmol) in 40 ml of dry dimethylformamide (DMF) was treated with 1,1′-carbonydidimidazole (CDI, 795 mg, 4.91 mmol) and stirred under nitrogen at room temperature for 1 hour. The N-ethyl N-(2-carbethoxy)ethyl amine linker 10 (1.90 g, 13.08 mmol) in 10 ml of dry dimethylformamide (DMF) was added dropwise and the reaction solution was stirred overnight at room temperature. The reaction solution was concentrated under reduced pressure and the resulting residue was dissolved in 200 ml of chloroform. The chloroform solution was washed twice with 100 ml of water, dried over anhydrous sodium sulphate, and concentrated under reduced pressure to yield the crude title compound 6 (2.2 g) as an oil. This was used without further purification in the following Example. υmax/cm−1 3121.90, 2987.10, 2848.65, 1735.30, 1676.97, 1202.97 (FT-IR: FIG. 9)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07115718B2 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-9fe6948392e045f8a8eb03a20c72f160 |
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| 출처 메모 | uspto-grants-2006_10 |
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