HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041867Generated: October 26, 2026
Dimethylamine, hydrochloride → 4-Dimethylamino-3-methanesulfonyl-benzoic acid methyl ester
https://huagongshe.com/reaction/1041867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4-Fluoro-3-(methylsulfonyl)benzoate | HCID 10752025 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Dimethylamino-3-methanesulfonyl-benzoic acid methyl ester | HCID 66909124 | 56% |
Reaction Steps
To a stirred solution of 5.23 g (22.5 mmol) 4-Fluoro-3-methanesulfonyl-benzoic acid methyl ester (J. Med. Chem.; 40; 13; 1997; 2017-2034) and 60.0 ml dimethylsulphoxid were added 2.23 g (27.0 mmol) dimethylamine hydrochloride and 6.54 g (47.3 mmol) potassium carbonate. The reaction mixture was stirred for 7 h at 60° C. in an autoclave and was concentrated with high vacuum rotation evaporator at 65° C. The residue was diluted with dichloromethane, washed twice with water. The combined water phases were extracted with dichloromethane. The combined dichloromethane phases were washed with diluted sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. The oily crude was purified by column chromatography and the desired product 10a was obtained in 56% yield (3.24 g, 12.6 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08557776B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-4e90e05250034a908ee44c51913f701b |
|---|
| Source note | uspto-grants-2013_10 |
|---|