참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 6-Bromoindole-3-carbaldehyde | HCID 2794830 | — |
| 반응물 | Tert-butyl Chloroformate | HCID 9920397 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | tert-butyl 6-bromo-3-formyl-1H-indole-1-carboxylate | HCID 11313330 | — |
반응 단계
6-Bromoindole-3-carboxaldehyde, 23 (5.0 g, 22.3 mmol) is dissolved in methylene chloride (40 mL), then cooled to 0° C. and tert-butylchloroformate (3.40 g, 25.0 mmol) and triethyl amine (2.50 g, 25.0 mmol) are added over 5 minutes. The reaction is maintained at reflux, under inert atmosphere for 3 hours. The reaction is cooled, filtered and the solvent removed in vacuo. The residue composed primarily of compound 24 is used in the Example 18 without purification. (See, e.g., G. Wille and W. Steglich, Synthesis, 2001, 759-762 for a related procedure.)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07964649B2 |
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| 출처 데이터셋 | uspto-grants-2011_06 |
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| ORD ID | ord-69c6fc11f5f84bed94d17a7a0a8b8255 |
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| 출처 메모 | uspto-grants-2011_06 |
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