Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HOAt → (r)-2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (2-phenyl 1-pyrrolidin-1-ylmethylethyl)amide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | HOAt | HCID 181649 | — |
| 반응물 | (r)-2-Phenyl-1-pyrrolidin-1-ylmethylethylamine | HCID 12184138 | — |
| 반응물 | 2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid | HCID 68703276 | — |
| 반응물 | EDCl H2O | HCID 87672115 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (r)-2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (2-phenyl 1-pyrrolidin-1-ylmethylethyl)amide | HCID 91139520 | — |
반응 단계
To a solution of the crude 2-cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (22 mg, step 74.5) in DMF (1.5 mL) are added (R)-2-phenyl-1-pyrrolidin-1-ylmethylethylamine (0.083 mmol), EDCl—H2O (0.11 mmol), and HOAt (0.11 mmol) at room temperature. The reaction mixture is stirred for 24 h and the reaction is quenched by the addition of H2O. The mixture is extracted with AcOEt, and the organic extracts are dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residue is purified by RP-HPLC to give the title compound; MS (M+1)+: 474, Rf (solvent): 0.63 (CH2Cl2:MeOH=10:1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07704996B2 |
| 출처 데이터셋 | uspto-grants-2010_04 |
| ORD ID | ord-ebbaec1b7fa74d20b57f0e984fa021c0 |
| 출처 메모 | uspto-grants-2010_04 |