HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → HCID 178466749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | (2R,3R)-2-(2,4-difluorophenyl)-3-[[1-(hydroxymethyl)-2-hydroxyethyl]-thio]-1-(1H-1,2,4-triazol-1-yl)-2-butanol | HCID 10594623 | — |
| Reactant | 4'-Acetyl-4-formylbenzanilide | HCID 18766324 | — |
| Product | HCID 178466749 | HCID 178466749 | 65% |
Reaction Steps
In the same manner as that described in Example 3(3), a reaction was carried out using 4′-acetyl-4-formylbenzanilide (200 mg, 0.75 mmol), (2R,3R)-2-(2,4-difluorophenyl)-3-[[1-(hydroxymethyl)-2-hydroxyethyl]thio]-1-(1H-1,2,4-triazol-1-yl)-2-butanol (256 mg, 0.71 mmol) and p-toluenesulfonic acid monohydrate (243 mg, 1.3 mmol) and the reaction mixture was treated according to a similar procedure to that described in Example 3(3) to give the trans isomer of the title compound (280 mg, yield 65%) as a white solid which was recrystallized from ethyl acetate-hexane to give white powdery crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06653330B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-95216602873140f6bebaf8695e2405b1 |
| Source note | uspto-grants-2003_11 |