참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Phenacyl bromide | HCID 6259 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | HCID 178479085 | HCID 178479085 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-Phenyl-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole | HCID 765511 | 90% |
반응 단계
Combine 2-iminopyrrolidine hydrochloride (6.98 g, 57.8 mmol) (Callahan, et al., J. Med. Chem. 45, 999-1001 (2002)), 2-bromoacetophenone (3.8 g, 19.3 mmol), and sodium carbonate (8.2 g, 77.2 mmol) in dry dimethylformamide (25 mL). Heat at 80° C. for 18 hours. Cool to room temperature, add water (60 mL), and extract with ethyl acetate (3×100 mL). Concentrate the combined organic layers under reduced pressure. Dilute the residue with diethyl ether (100 mL), wash with cold water (3×80 mL), and concentrate under reduced pressure to provide the desired compound as a white solid (3.2 g, 89%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07863310B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-86e038ca51c64e73b5384b65ff45a87a |
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| 출처 메모 | uspto-grants-2011_01 |
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