HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 4-(Tert-butylcarbamoyl)-2-methoxybenzenesulphonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-Chlorosulfonyl-3-methoxybenzoyl chloride | HCID 10492173 | — |
| Reactant | 3-Methoxy-4-sulfobenzoic acid mono-potassium salt | HCID 88010997 | — |
| Product | 4-(Tert-butylcarbamoyl)-2-methoxybenzenesulphonyl chloride | HCID 9926536 | 92% |
Reaction Steps
Reacting the 3-methoxy-4-sulfobenzoic acid mono-potassium salt with an inorganic acid halogenide the 4-chlorosulfonyl-3-methoxybenzoyl chloride is obtained. To our surprise we have found that at lower temperature, in an appropriate solvent the t-butylamine reacts selectively with the aromatic acid chloride. Thus, the desired 2-methoxy-4-(N-t-butylaminocarbonyl)benzenesulfonyl chloride is obtained in 92% yield, with a purity of 96%, so it can be used without further purification for the synthesis of drug substances.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548702B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-1148356fbc3f4458a93bd7f6fdbdf4e6 |
| Source note | uspto-grants-2003_04 |