HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indazole-3-carboxylic acid, 1-methyl- → 1-Methyl-1H-indazole-3-carboxylic acid{2-[5-(3,4-dichlorophenyl)furan-2-yl]ethyl}amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indazole-3-carboxylic acid, 1-methyl- | HCID 689105 | — |
| Reactant | 2-(5-(3,4-Dichlorophenyl)furan-2-yl)ethanamine hydrochloride | HCID 67168344 | — |
| Product | 1-Methyl-1H-indazole-3-carboxylic acid{2-[5-(3,4-dichlorophenyl)furan-2-yl]ethyl}amide | HCID 67172132 | — |
Reaction Steps
The title compound was prepared as in Example 12 starting from N-methyl-indazole-3-carboxylic acid and 2-[5-(3,4-dichlorophenyl)furan-2-yl]ethylamine hydrochloride. The crude product was purified by flash chromatography using heptane/EtOAc as a gradient eluent (9:1-8:2). 1H NMR (400 MHz, DMSO-d6): 3.00 (2H, t), 3.64 (2H, m), 4.12 (3H, s), 6.36 (1H, d), 7.01 (1H, d), 7.26 (1H, m), 7.46 (1H, m), 7.600 (1H, s), 7.602 (1H, s), 7.72 (1H, d), 7.83 (1H, s), 8.16 (1H, d), 8.48 (1H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975254B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-d28926f872674613a54aeb5b5f93d266 |
| Source note | uspto-grants-2015_03 |