HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenylmethane bromide → 3-[(2-Diphenylmethylthio-4,5-dihydronaphtho[1,2-d]thiazol-6-yl)oxy]propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenylmethane bromide | HCID 18470978 | — |
| Reactant | HCID 178472162 | HCID 178472162 | — |
| Product | 3-[(2-Diphenylmethylthio-4,5-dihydronaphtho[1,2-d]thiazol-6-yl)oxy]propionic acid | HCID 18471014 | 39% |
Reaction Steps
Using ethyl 3-[(2-mercapto-4,5-dihydronaphtho[1,2-d]thiazol-6-yl)oxy]propionate and diphenylmethane bromide, the procedure of Example 21 was otherwise repeated to synthesize the title compound. Yield 39%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248766B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-a9a9a9fd4d0c461c9a68f80ba726ba83 |
| Source note | uspto-grants-2001_06 |