HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indazole-3-carbonyl chloride → N-((quinuclidin-4-yl)methyl)-1H-indazole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indazole-3-carbonyl chloride | HCID 23189990 | — |
| Reactant | N-((quinuclidin-4-yl)methyl)-1H-indole-3-carboxamide | HCID 25210594 | — |
| Product | N-((quinuclidin-4-yl)methyl)-1H-indazole-3-carboxamide | HCID 25234268 | — |
Reaction Steps
N-((quinuclidin-4-yl)methyl)-1H-indazole-3-carboxamide was prepared in a similar manner to N-((quinuclidin-4-yl)methyl)-1H-indole-3-carboxamide, substituting 1H-indazole-3-carbonyl chloride as the electrophile. 1HNMR: 13.6 (bs, 1H); 9.65 (bs, 1H); 8.45 (t, 1H); 8.15 (d, 1H); 7.62 (d, 1H); 7.41 (t, 1H); 7.2 (t, 1H); 3.28 (m, 2H); 3.21 (m, 6H); 1.70 (m, 6H). MS (m/e): 285.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114891B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-bea88cfc64a7497391dc3a2944a5a6a6 |
| Source note | uspto-grants-2012_02 |