HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-chloro-1-phenyl-1H-indole-3-carbaldehyde → HCID 86596811, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-chloro-1-phenyl-1H-indole-3-carbaldehyde | HCID 314793 | — |
| Reactant | HCID 67371144 | HCID 67371144 | — |
| Product | HCID 86596811 | HCID 86596811 | 37% |
Reaction Steps
2-Chloro-1-phenyl-1H-indole-3-carboxaldehyde is reacted with [1,4,7]triazocane as described in Example 1 to afford 1-phenyl-2-[1,4,7]triazocan-1-yl-1H-indole-3-carboxaldehyde (37% yield) as a yellow solid. LC/MS: 321 (M+H—H2O); RT 2.96 min; NMR (CDCl3): 7.37 (1H, d), 7.18-7.30 (3H, m), 7.13 (1H, t), 6.97 (2H, d), 6.90 (1H, t), 6.79 (1H, t), 2.76-3.10 (12H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405300B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-af22fed0de074aeda9fc8442c463eb0a |
| Source note | uspto-grants-2008_07 |