HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanesulfonic acid → Ethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanesulfonic acid | HCID 11668 | — |
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | Alvelestat tosylate | HCID 46861622 | — |
| Product | Ethanesulfonate | HCID 3717105 | — |
| Product | Alvelestat tosylate | HCID 46861622 | — |
Reaction Steps
Compound (I) esylate was synthesized using an analogous method to that described for the synthesis of compound (I) tosylate in Example 8a from compound (I) (50 mg, 0.092 mmol) and ethane sulfonic acid (9.3 mg, 0.092 mmol). No precipitation was obtained after stirring over night. The solvent was evaporated and ethyl acetate (2 ml) was added. A suspension was formed. The suspension was stirred over night, was filtered and dried under vacuum at 50° C. to give the title product; yield 49 mg, 0.075 mmol, 81%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232296B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-be4bb7e22e7d4d26a7efb2299457b5af |
| Source note | uspto-grants-2012_07 |