HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984441Generated: October 29, 2026
Cyclohexanecarboxaldehyde → HCID 22558437, compound
https://huagongshe.com/reaction/984441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Acetic acid methylene chloride | HCID 21922555 | — |
| Reactant | HCID 22558368 | HCID 22558368 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22558437 | HCID 22558437 | — |
Reaction Steps
A stirred solution of 48 mg of N-[3-methoxy-4-(5-oxazolyl)phenyl]-N′-[1,1-dimethyl-2-(1-piperazinyl)ethyl]oxalamide (1.2 mmol) and 13 mg of cyclohexanecarboxaldehyde (1.2 mmol) in 1 ml of a 5% acetic acid/dichloromethane mixture was treated with a solution of 38 mg of sodium triacetoxyborohydride (1.8 mmol) in 1 ml of a 5% acetic acid/dichloromethane mixture. After stirring overnight at room temperature the reaction mixture was diluted with 10 ml of dichloromethane and washed with 8 ml of a sodium bicarbonate solution followed by 8 ml of water. The organic layer was then evaporated and purified using flash chromatography on a silica gel column eluting with 5% methanol/dichloromethane to give after evaporation of the fractions 14.3 mg (0.3 mmol, 25%) of N-[2-[4-(cyclohexylmethyl)-1-piperazinyl-1,1-dimethylethyl]-N′-[3-methoxy-4-(5-oxazolyl)phenyl]oxalamide in the form of a white solid. MS: m/e 498.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06867299B2 |
|---|
| Source dataset | uspto-grants-2005_03 |
|---|
| ORD ID | ord-58b5b70373ff484fa17127d5319457a0 |
|---|
| Source note | uspto-grants-2005_03 |
|---|