HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonate → Methyl p-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | KD-3010 | HCID 16048651 | — |
| Product | Methyl p-toluenesulfonate | HCID 6645 | — |
| Product | p-Toluenesulfonate | HCID 85570 | — |
Reaction Steps
The methyl ester precursor of (S)-4-[cis-2,6-dimethyl-4-(4-trifluoromethoxy-phenyl)-piperazine-1-sulfonyl]-indan-2-carboxylic acid tosylate (hereinafter optionally referred to as “Compound 1 tosylate”) was used for this experiment instead of Compound 1 tosylate due to the unsuitability of the Compound 1 tosylate crystals for X-ray structure determination. Compound 1 tosylate methyl ester was prepared via an esterification of Compound 1 tosylate followed by recrystallization from isopropanol. Other experiments have established that the stereochemistry is retained in converting the methyl ester to Compound 1 tosylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863276B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-a67dd3abc5b34ca3b4a0be879f6a7f7a |
| Source note | uspto-grants-2011_01 |