Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-(tert-Butyl)-2-(tributylstannyl)pyridine → 2-(4-Methylcarbamoyl-pyridin-2-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-(3-cyano-azetidin-1-yl)-1-methyl-2-oxo-ethyl]-amide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-(tert-Butyl)-2-(tributylstannyl)pyridine | HCID 57516631 | — |
| 반응물 | N-methyl-2-tributylstannanyl-isonicotinamide | HCID 57516644 | — |
| 반응물 | 2-Bromo-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-(3-cyano-azetidin-1-yl)-1-methyl-2-oxo-ethyl]amide | HCID 58438612 | — |
| 반응물 | 2-bromo-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-(4-cyano-piperidin-1-yl)-1-cyclopropyl-2-oxo-ethyl]-amide | HCID 86657873 | — |
| 생성물 | 2-(4-Methylcarbamoyl-pyridin-2-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-(3-cyano-azetidin-1-yl)-1-methyl-2-oxo-ethyl]-amide | HCID 53385691 | — |
반응 단계
Prepared according to the procedure outlined in Example 111, steps 4-5 substituting 2-bromo-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-(3-cyano-azetidin-1-yl)-1-methyl-2-oxo-ethyl]-amide for 2-bromo-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-(4-cyano-piperidin-1-yl)-1-cyclopropyl-2-oxo-ethyl]-amide and N-methyl-2-tributylstannanyl-isonicotinamide for 4-tert-butyl-2-(tributylstannyl)pyridine. MS: (M+H)+=433.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08518945B2 |
| 출처 데이터셋 | uspto-grants-2013_08 |
| ORD ID | ord-837e2afe4c8f4946be468eaa4471ff3b |
| 출처 메모 | uspto-grants-2013_08 |