HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042317Generated: November 1, 2026
Potassium tert-butoxide → HCID 58133378, compound
https://huagongshe.com/reaction/1042317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 58133380 | HCID 58133380 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58133378 | HCID 58133378 | — |
Reaction Steps
To a solution of 2-{[2-(2,6-diethyl-4-methyl-phenyl)-acetyl]-methyl-amino}-nicotinic acid methyl ester (300 mg) in N,N-dimethylformamide (5 ml) was added potassium tert-butoxide (250 mg). The reaction mixture was stirred at ambient temperature for 18 hours, and then at 50° C. for 2 hours. The reaction mixture was partitioned the reaction between water and dichloromethane. The phases were separated and the aqueous phase was extracted with further dichloromethane and ethyl acetate. The aqueous phase was acidified by addition of aqueous hydrochloric acid (2M) and extracted three times with ethyl acetate. The combined organic extracts were dried over magnesium sulfate and concentrated. The residue was passed through a plug of silica eluting with ethyl acetate to give Compound No. D20 of Table D as an off-white solid (320 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08557840B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-3522a1d9ae62482d8229d41c69af4b0b |
|---|
| Source note | uspto-grants-2013_10 |
|---|