HuagongsheHuagongshe Chemistry Print Report · For research reference only
HOAt → (r)-2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (2-phenyl 1-pyrrolidin-1-ylmethylethyl)amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HOAt | HCID 181649 | — |
| Reactant | (r)-2-Phenyl-1-pyrrolidin-1-ylmethylethylamine | HCID 12184138 | — |
| Reactant | 2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid | HCID 68703276 | — |
| Reactant | EDCl H2O | HCID 87672115 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (r)-2-Cyano-4-(spiro[2.5]oct-6-ylmethyl)pyrimidine-5-carboxylic acid (2-phenyl 1-pyrrolidin-1-ylmethylethyl)amide | HCID 91139520 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07704996B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-ebbaec1b7fa74d20b57f0e984fa021c0 |
| Source note | uspto-grants-2010_04 |