참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methyl 2,5-Dichloronicotinate | HCID 2764318 | — |
| 반응물 | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| 반응물 | Tert-butyl 3-(3-fluorophenyl)-3-hydroxyazetidine-1-carboxylate | HCID 65918384 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | MeOH tetrahydrofuran | HCID 21899815 | — |
| 생성물 | Methyl 5-chloro-2-(3-(3-fluorophenyl)-3-hydroxyazetidin-1-yl)nicotinate | HCID 67958212 | 56.7% |
반응 단계
To a cooled (0° C.) solution of tert-butyl 3-(3-fluorophenyl)-3-hydroxyazetidine-1-carboxylate (D28) (100 mg, 0.374 mmol) in dichloromethane (0.5 ml), a mixture 3:1 of trifluoroacetic acid/dichloromethane (1 ml) was added and the mixture was stirred 30 min at room temperature. The residue obtained after solvent evaporation was dissolved in a mixture 3:1 of tetrahydrofuran/methanol (1 ml) and triethylamine (0.156 ml, 1.122 mmol) was added followed by addition of methyl 2,5-dichloronicotinate (77.32 mg, 0.374 mmol). The resulting mixture was heated 15 h at 60° C. After solvent evaporation the residue was taken in NH4Cl sat. sol. (10 ml) and the resulting mixture was extracted with ethylacetate (2×10 ml). The residue obtained after solvet evaporation was purified by SPE-Si cartridge (5 g) eluting with a mixture cyclohexane/ethylacetate from 100/0 to 90:10. Collected fractions, after solvent evaporation afforded the title compound (D80) (71.4 mg)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08828987B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-a2dc3b146bfc435393ab564a73b8fb2f |
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| 출처 메모 | uspto-grants-2014_09 |
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