Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | (R)-3,3-Dimethyl-2-aminobutane | HCID 5324845 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | ethyl 1-(2-bromoethyl)-3-(phenoxymethyl)-1H-pyrazole-5-carboxylate | HCID 67974304 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67976139 | HCID 67976139 | 233.7% |
| Product | HCID 67991632 | HCID 67991632 | — |
Reaction Steps
(R)-3,3-Dimethyl-2-aminobutane (0.37 g, 2.86 mmol) was added to a suspension of 2-(2-bromoethyl)-5-phenoxymethyl-2H-pyrazole-3-carboxylic acid ethyl ester (0.1 g, 0.28 mmol) and potassium iodide (9 mg, 0.056 mmol) in ACN (1 mL). The mixture was stirred at 90° C. for 20 hours. Sodium tert-butoxide (41 mg, 0.42 mmol) and DMF (1 mL) was added and the mixture was stirred at 130° C. for 20 minutes under microwave irradiation. The solvent was evaporated in vacuo. The crude product was washed with a 2N solution of HCl until pH 1 and extracted with AcOEt. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo to yield a 1:1 mixture (R)-5-phenoxymethyl-2-[2-(1,2,2-trimethyl-propylamino)-ethyl]-2H-pyrazole-3-carboxylic acid ethyl ester and (R)-5-phenoxymethyl-2-[2-(1,2,2-trimethyl-propylamino)-ethyl]-2H-pyrazole-3-carboxylic acid (113 mg, 57%) as a yellow oil which was used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592422B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-4e3feca790eb4caa95c275f0a27d50b1 |
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| Source note | uspto-grants-2013_11 |
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