HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromofuran-2-carbohydrazide → 1-{[5-(5-Bromo-2-furanyl)-1,3,4-oxadiazol-2-yl]methyl}-4-(trifluoromethyl)-1H-indole-5-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromofuran-2-carbohydrazide | HCID 468636 | — |
| Reactant | [5-cyano-4-(trifluoromethyl)-1H-indol-1-yl]acetic acid | HCID 57800132 | — |
| Product | 1-{[5-(5-Bromo-2-furanyl)-1,3,4-oxadiazol-2-yl]methyl}-4-(trifluoromethyl)-1H-indole-5-carbonitrile | HCID 24984782 | — |
Reaction Steps
Synthesized as described in Example 35C from [5-cyano-4-(trifluoromethyl)-1H-indol-1-yl]acetic acid and 5-bromo-2-furancarbohydrazide: MS (ES) m/z 437 and 439 (M+1 Br isotopes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572820B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-cf53012831014d8ca378e74a89785947 |
| Source note | uspto-grants-2009_08 |