Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178522341 | HCID 178522341 | 87.7% |
Reaction Steps
3-Aminopyrazole (9 g, 108 mmol) was dissolved in DCM (250 ml). N-methylmorpholine (26.5 g, 262 mmol) was added in one portion. Benzoyl chloride (34.86 g, 248 mmol) was added slowly at room temperature. After stirring at room temperature for 16 hours, the mixture was concentrated under reduced pressure to give a solid. The solid was dissolved in methanol (200 ml). Aqueous solution of NaOH (2.5M, 120 ml, 300 mmol) was added slowly, and THF (50 ml) was added in order to obtain a homogeneous solution. After stirring at room temperature for 20 minutes, the mixture was concentrated under reduced pressure and poured into water (300 ml). The precipitate was filtered and dried in an oven to afford 17.55 g light yellow solid, the yield was 87.7%. 1H-NMR (400 MHz, d6-DMSO): δ 12.45 (s, 1H), 10.79 (s, 1H), 7.99-8.02 (m, 2H), 7.67 (s, 1H), 7.48-7.59 (m, 3H), 6.65 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388168B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-1d7c88f9e45c4257b20e82e6a38a485e |
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| Source note | uspto-grants-2016_07 |
|---|