HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminoisobutyric acid → 5-Isopropylamino-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-chloro-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide | HCID 25013543 | — |
| Product | 5-Isopropylamino-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide | HCID 25013378 | — |
Reaction Steps
Heating a mixture of 5-chloro-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (Example 5, 88 mg; 0.30 mmol), triethylamine (0.43 mL; 3.1 mmol) and 2-aminoisobutyric acid (320 mg; 3.1 mmol) under microwave irradiation for 6 hr according to the procedure described for Example 14 provided after purification by reverse phase HPLC, 5-isopropylamino-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (28 mg, 29%) as an off-white powder. ES-HRMS m/e calcd for C18H29N4O (M+H+) 317.2336, found 317.2334.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728029B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-998eec4678a34453b962037b0f34f3c6 |
| Source note | uspto-grants-2010_06 |