HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole-5-carbonitrile → (3-Acetyl-5-cyano-indol-1-yl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole-5-carbonitrile | HCID 27513 | — |
| Reactant | (3-Acetyl-5-trifluoromethoxy-indol-1-yl)acetic acid | HCID 68284505 | — |
| Product | (3-Acetyl-5-cyano-indol-1-yl)-acetic acid | HCID 68284791 | — |
Reaction Steps
was prepared from 1H-indole-5-carbonitrile in a similar manner as described in Scheme A13 for the preparation of (3-acetyl-5-trifluoromethoxy-indol-1-yl)-acetic acid. MS (LC/MS): 241.2 [M−H]−; 243.2 [M+H]+; tR (HPLC conditions a): 2.62 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09085555B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-3cea69c62dd84b238bd3f3f27e69df70 |
| Source note | uspto-grants-2015_07 |