HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 46200667, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | 2-((2-(4-(Oxazol-5-yl)phenylamino)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)(phenyl)amino)ethanol | HCID 46200050 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 46200667 | HCID 46200667 | 18.4% |
Reaction Steps
2-((2-(4-(Oxazol-5-yl)phenylamino)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)(phenyl)amino)ethanol (100 mg, 0.23 mmol, Example 1) was dissolved in MeOH (0.5 mL) and dichloromethane (5 mL). Triethylamine (0.033 mL, 0.23 mmol) was added followed by ethanesulphonyl chloride (0.022 mL, 0.23 mmol). The reaction mixture was stirred at room temperature for 1 h before the solvent was evaporated under reduced pressure. The crude was dissolved in dimethylformamide and acetonitrile and purified by preparative HPLC yielding 2-((6-(ethylsulfonyl)-2-(4-(oxazol-5-yl)phenylamino)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)(phenyl)amino)ethanol (22.0 mg, 18.11%). MS (ESI) (M+1) m/z 521;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188101B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-6b782054cd394fd9ae83d4df8e2fb67f |
| Source note | uspto-grants-2012_05 |