HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501349Generated: November 4, 2026
Diisopropylethylamine → HCID 70856688, compound
https://huagongshe.com/reaction/1501349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamate | HCID 86691038 | — |
| Reactant | 6-Ethoxy-4,5-dimethylpyridazin-3-amine | HCID 86716518 | — |
| Solvent | Butyronitrile | HCID 8008 | — |
| Product | HCID 70856688 | HCID 70856688 | 70% |
Reaction Steps
A mixture of crude tert-butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamate [that was prepared in a manner analgous to that described for Intermediate Example Int-1-A] (300 mg, ˜80% purity, 0.540 mmol, 1.0 eq), 6-ethoxy-4,5-dimethylpyridazin-3-amine (that was prepared in a manner analgous to that described for Intermediate Example Int-36, Step 1, 124 mg, ˜80% purity, 0.590 mmol, 1.1 eq) and N,N-diisopropylethylamine (100 μL, 0.590 mmol, 1.1 eq) in butyronitrile (3.3 mL) was heated for 3.5 hours at 125° C. On cooling the reaction mixture was concentrated in vacuo. The crude mixture was purified via preparative MPLC (Biotage Isolera; 50 g SNAP-cartridge: hexane/EtOAc 9/1→hexane/EtOAc 1/1) to give 220 mg (70% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206185B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-27e3408ce6f4476db8da9dbec11e0df6 |
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| Source note | uspto-grants-2015_12 |
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