HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl (cyanomethyl)phosphonate → HCID 70562878, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 86705043 | HCID 86705043 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70562878 | HCID 70562878 | — |
Reaction Steps
To a mixture of diethyl cyanomethylphosphonate (145 mg, 0.76 mmol), LiCl (43 mg, 1.01 mmol) and DBU (255 mg, 1.01 mmol) in acetonitrile (15 mL) was added a solution of tert-butyl 1-(2-(4-chlorophenyl)-1-oxobutan-2-yl)-1H-indol-4-ylcarbamate (210 mg, 1.02 mmol), as described in Example 21 Step B, in acetonitrile (3 mL). The mixture was stirred at room temperature for 2 h and the volatile was evaporated. The residue was purified by silica gel chromatography eluting with PE/EA (10/1 to 3/1, v/v) to afford the title compound as a white solid. LC/MS m/z=458.1 [M+Na]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403807B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-d07d83cc93fb424dbdc02665e66d1c98 |
| Source note | uspto-grants-2016_08 |