HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454339Generated: October 30, 2026
Diisopropylethylamine → HCID 178496584, compound
https://huagongshe.com/reaction/454339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(3,5-dibromopyrazin-2-yl)-2-iodoacetamide | HCID 58298325 | — |
| Reactant | HCID 178496582 | HCID 178496582 | — |
| Reactant | HCID 178496610 | HCID 178496610 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178496584 | HCID 178496584 | 55% |
Reaction Steps
6-Bromo-4-((cis)-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one. To a solution of N-(3,5-dibromopyrazin-2-yl)-2-iodoacetamide (See Example 5.B) (1.0 g, 2.376 mmol) and diisopropylethylamine (1.038 mL, 5.94 mmol) in acetonitrile (10 mL) was added (cis)-4-methoxycyclohexanamine hydrochloride (0.413 g, 2.495 mmol). The solution was stirred at 55° C. for 3 h. The resulting precipitate was filtered and washed with acetonitrile and dried under reduced pressure to afford the title compound (0.442 g, 1.29 mmol, 55% yield). MS (ESI) m/z 341.3 [M]+, 343.3 [M+2]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492381B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-d2cb957335d545d592434b621fafad46 |
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| Source note | uspto-grants-2013_07 |
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