참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | Chloromethyl Methyl Ether | HCID 7864 | — |
| 반응물 | 5-(Bromomethyl)-3-methoxy-1,2-oxazole | HCID 10845405 | — |
| 반응물 | 3-Diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazole | HCID 22906284 | — |
| 반응물 | HCID 178462446 | HCID 178462446 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Propiolic Acid | HCID 10110 | — |
| 생성물 | HCID 178462446 | HCID 178462446 | — |
반응 단계
Dibromoolefin intermediate XIX is then converted to ethynyl intermediate XX. Treatment of the dibromoolefin intermediate with about two equivalents of n-butyllithium produces the lithium acetylide XX, wherein R13 is Li. This transformation is typically carried out in a polar organic solvent, such as tetrahydrofuran, at a temperature of about -78° C. to about 25° C. The lithium acetylide is reacted with electrophiles, such as methoxymethyl chloride, 5-bromomethyl-3-methoxyisoxazole, 3-diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazole, carbon dioxide, tetrazole disulfide, and the like, to prepare the formula I compounds. In a typical example, the lithium acetylide is treated with solid CO2 at a temperature of about -78° C. to about -60° C. to produce propargylic acid intermediate XX wherein R13 is CO2H. This compound may be further modified as described herein.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05606062 |
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| 출처 데이터셋 | uspto-grants-1997_02 |
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| ORD ID | ord-574031d5700748da82256e72eb159a91 |
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| 출처 메모 | uspto-grants-1997_02 |
|---|