HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494153Generated: October 30, 2026
Semicarbazide hydrochloride → HCID 68864498, compound
https://huagongshe.com/reaction/494153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86624802 | HCID 86624802 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68864498 | HCID 68864498 | — |
Reaction Steps
A solution of crude 4-bromoacetyl-10-(benzyloxy)-2-(3-chloro-4-fluorobenzyl)-8-methyl-7,8-dihydropyrazino[1′,2′:1,5]pyrrolo[2,3-d]pyridazine-1,9(2H,6H)-dione (1.25 g, 2.13 mmol) in anhydrous THF, semicarbazide hydrochloride (0.35 g, 3.14 mmol), and diisopropylethylamine (0.66 mL, 3.77 mmol) was heated in a sealed tube at 100° C. for 30 minutes. The reaction mixture was concentrated under vacuum. The residue was dissolved in DMSO and subject to reverse phase preparative HPLC purification. Collection and lyophilization of appropriate fraction provided the intermediate 2-{2-[10-(benzyloxy)-2-(3-chloro-4-fluorobenzyl)-8-methyl-1,9-dioxo-1,2,6,7,8,9-hexahydropyrazino[1′,2′:1,5]pyrrolo[2,3-d]pyridazin-4-yl]-2-oxoethyl}hydrazinecarboxamide as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538112B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-db89dd42e80d45f08f51572de3056c47 |
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| Source note | uspto-grants-2009_05 |
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