HuagongsheHuagongshe Chemistry Print Report · For research reference only
D-Proline → Chloro(1-quinolin-6-ylcyclopropyl)acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | D-Proline | HCID 8988 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (1-Quinolin-6-ylcyclopropyl)acetaldehyde | HCID 86621505 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Chloro(1-quinolin-6-ylcyclopropyl)acetaldehyde | HCID 86621504 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a mixture of (1-quinolin-6-ylcyclopropyl)acetaldehyde (410 mg, 1.94 mmol), D-proline (45 mg, 0.39 mmol) in dichloromethane (10 mL) cooled (0° C.) was added N-chlorosuccinimide (311 mg, 2.33 mmol) with stirring. The reaction mixture was stirred at 0° C. for 1 h, then gradually warmed to RT. The reaction mixture was quenched with water, extracted with dichloromethane. The combined organic extracts were concentrated and the residue purified by flash chromatography eluting with ethyl acetate in hexanes (0-25% in 18 min) to afford the desired product. (320 mg, 67.1%) LCMS: (M+H)=246.2; (M+H2O+H)=264.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767675B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-633c4f352ebe4a3996cfe242058e6945 |
| Source note | uspto-grants-2010_08 |