Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-[4-(Propan-2-yl)piperazin-1-yl]pyrazine | HCID 20613839 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67145119 | HCID 67145119 | — |
Reaction Steps
4-Isopropyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (1.0 g, 4.8 mmol) was dissolved in dichloromethane (30 mL) and the solution was placed on an ice-bath and brominated according to literature (Tetrahedron 44, 10, 1988, 2977-2984) in very bad yield. N-Bromosuccinimide (3.45 g, 19.4 mmol) was added slowly at 0° C. and then left overnight at rt. No reaction was observed. An additional 3.45 g of N-bromosuccinimide was added during 8 h, and then the reaction mixture was left at rt for 2 days. Aqueous concentrated Na2CO3 was added and the mixture was extracted with dichloromethane (3×75 mL). The combined organic extracts were dried (MgSO4), filtered and evaporated. The oily residue was purified on a silica gel column with dichloromethane/MeOH (9:1) as eluent. Yield: 196 mg (28%) of 5-bromo-4-isopropyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501739B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-6cd2b2cc1c354cf2b6b984f921062d58 |
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| Source note | uspto-grants-2013_08 |
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