Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Reactant | HCID 178507266 | HCID 178507266 | — |
| Solvent | Methyl Chloride | HCID 6327 | — |
| Product | HCID 178521739 | HCID 178521739 | 78% |
Reaction Steps
122 mg (loading 1.91 mmol/g, 0.233 mmol) of polystyrene supported N-methylmorpholine were suspended in 4 ml of chloromethane and then treated with 25.6 mg (0.117 mmol) of 4-bromobenzoyl chloride followed by 4.8 mg (0.039 mmol) of 3-cyclopropyl-5-amino-pyrazole. After 48 hours under stirring at room temperature the resin was separated by filtration and washed with 2 ml of dichloromethane. The filtrate was evaporated to dryness, the residue re-dissolved in 4 ml of dichloromethane and 100 mg of polystyrene supported trisamine were added. After 48 hours or stirring at room temperature the resin was filtered, washed with 2 ml of dichloromethane and concentrated to give, after triturating with diethylether, 9.3 mg (78% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07034049B1 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-8d58305e75a74c79be5f8ed5fd6d45f7 |
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| Source note | uspto-grants-2006_04 |
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