HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 86729393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86729391 | HCID 86729391 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 86729393 | HCID 86729393 | — |
Reaction Steps
To a suspension of 3-[4-carbamoyl-3-(phenylamino)-1H-pyrazol-1-yl]-3-(cyanomethyl)azetidinium trifluoroacetate (Intermediate #38-2) (50 mg, 0.17 mmol) in DCE (2.0 mL) was added sodium triacetoxyborohydride (79 mg, 0.37 mmol), followed by formaldehyde (0.050 mL, 0.67 mmol, 37 wt % in water). The resulting mixture was allowed to stir for 1 hour before saturated aqueous NaHCO3 solution was added and the resulting mixture was extracted with EtOAc (3×). The combined organic layers were dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 0-100%, EtOAc/hexanes) to afford the title compound, Example #20.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328099B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-073395f4bc5c41d1b7254b17b45aa610 |
| Source note | uspto-grants-2016_05 |