HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 77709006, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733286 | — |
| Reactant | HCID 11414215 | HCID 11414215 | — |
| Reactant | HCID 17901841 | HCID 17901841 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 77709006 | HCID 77709006 | 110.3% |
Reaction Steps
To 3-(4-cyano-phenyl)-2-(R,S)-cyclohexyl-propionic acid (5 g, 19.43 mmol) and (cyclohexylmethyl-amino)-acetic acid tert-butyl ester (4.42 g, 19.43 mmol) in dimethylformamide (50 ml) were added TOTU (7.01 g, 21.37 mmol) and diisopropylethyl amine (2.51 g, 19.43 mmol) at −15° C. The mixture was stirred for 1 hour and then allowed to warm to room temperature. After evaporation, the residue was treated with sodium bicarbonate solution and extracted with ethyl acetate. The organic layer was evaporated to yield 10 g of crude material which was used in the next step without further purification, MS m/z: 467.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06759420B1 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-d3b55f44a1324895bedbcf35c4a2f8ee |
| Source note | uspto-grants-2004_07 |