참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tyramine | HCID 5610 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Bis(2-chloroethyl)amine | HCID 9533 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| 반응물 | Methyl chloromethanethioate | HCID 554404 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | bis-(2-Chloroethyl)amino-4-hydroxyphenylaminomethanone | HCID 21091234 | — |
반응 단계
One pot method. bis-(2-Chloroethyl)amine hydrochloride 26 (200 mg, 1.1 mmol) was dissolved in dichloromethane (15 mL) and triethylamine (0.45 mL, 3.3 mmol) was added. The mixture was stirred for 5 minutes at ambient temperature and ethyl chloroformate or methyl chlorothioformate (1.32 mmol) was added. The mixture was stirred until no bis-(2-chloroethyl)amine remained by TLC (ethyl acetate). Tyramine (300 mg, 2.2 mmol) was added and the mixture was heated under reflux for 4 hours. the mixture was allowed to cool, purified by dry flash column chromatography (silica gel, dichloromethane 200 cm3) and concentrated in vacuo to yield prodrug 28 as an orange/brown oil (234 mg, 67% for methyl chlorothioformate and 229 mg, 64% for ethyl chloroformate).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07183319B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-6f87aab0f5034d669aca154b543b3923 |
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| 출처 메모 | uspto-grants-2007_02 |
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