HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027302Generated: October 29, 2026
3,6-Dichloropyridazine → HCID 44190436, compound
https://huagongshe.com/reaction/1027302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Cis-2-boc-hexahydropyrrolo[3,4-C]pyrrole | HCID 1514452 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44190436 | HCID 44190436 | 70.3% |
Reaction Steps
To a solution of 3,6-dichloropyridazine (462 mg, 3.10 mmol) in n-butanol (8 mL) was added DIPEA (1.354 ml, 7.75 mmol) and (3aR,6aS)-tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (658 mg, 3.1 mmol). The reaction mixture was heated at 120° C. for 2 hour, and then diluted with DCM and water. The organic layer was separated and concentrated to a brownish oil, which was purified by silica gel chromatography (0-25% EtOAc/DCM) to afford (3aR,6aS)-tert-butyl 5-(6-chloropyridazin-3-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (730 mg, 2.180 mmol, 70% yield), MS (M+1)=325.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729263B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-940abd539faf42b2a2fd8884419adffe |
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| Source note | uspto-grants-2014_05 |
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