참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | N-(2-bromoethyl)methanesulfonamide | HCID 285330 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Ether methanol ammonium hydroxide | HCID 131726330 | 26% |
반응 단계
To a solution of compound (AFD) (0.40 mmol) in dry DMF was added triethylamine (0.45), followed by the alkylating agent Br(CH2)2NHSO2CH3 (0.45 mmol). The resulting mixture was stirred at 80° C. overnight. After completion of the reaction, the cooled mixture was poured into 1M NaOH (150 mL) and extracted with ethyl acetate (2×100 mL). The organic extracts were dried (MgSO4) and the solvent evaporated at the rotary evaporator to leave a gum. Flash chromatography of the residue (SiO2, ether:methanol:ammonium hydroxide (200:10:1)) provided compound (AFV) as a colorless gum: (yield:26%); purity >97% (HPLC); MS: m/z 616.3 (M+1); 1H NMR (DMSO d6): δ 2.1–2.2 (br s, 3H), 2.3–2.4 (m, 5H), 2.75 (s, 3H) 2.9–2.10 (br s, 3H), 3.3–3.4 (m, 6H), 3.5 (m, 3H), 4.65 (m, 2H), 7.15–7.5 (m, 16H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07202259B2 |
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| 출처 데이터셋 | uspto-grants-2007_04 |
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| ORD ID | ord-7f259a7924fd41cca8357dc53868666d |
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| 출처 메모 | uspto-grants-2007_04 |
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