HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethyl methyl ether → HCID 57944971, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | HCID 57422493 | HCID 57422493 | — |
| Product | HCID 57944971 | HCID 57944971 | 20% |
Reaction Steps
Prepared as in example 10-91 from 1-benzyl-4-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1,2,4-triazolidine-3,5-dione (example 10-91a) and 2-bromoethyl methyl ether. Yield: 20%. MS M+H calculated 425.19; found 425.2. The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 0.06 μM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939671B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-de1fdddb85ef4af2a9131aec826fd9f2 |
| Source note | uspto-grants-2011_05 |