HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501343Generated: November 3, 2026
Diisopropylethylamine → HCID 86716516, compound
https://huagongshe.com/reaction/1501343
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Amino-6-chloro-4,5-dimethylpyridazine | HCID 6991943 | — |
| Reactant | tert-Butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamate | HCID 86691038 | — |
| Solvent | Butyronitrile | HCID 8008 | — |
| Product | HCID 86716516 | HCID 86716516 | 78% |
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] (237 mg, ˜80% purity, 0.430 mmol, 1.0 eq), 6-chloro-4,5-dimethylpyridazin-3-amine (CAS-Nr. 76593-36-7, 67.2 mg, 0.430 mmol, 1.0 eq) and N,N-diisopropylethylamine (70 μL, 0.430 mmol, 1.0 eq) in butyronitrile (2.6 mL) was heated for 17 hours at 125° C. On cooling the mixture was partitioned between DCM and water, stirred vigorously and filtered through a silicone coated filter paper. The filtrate was concentrated in vacuo. The crude mixture was purified via MPLC (Biotage Isolera; 25 g SNAP cartridge: hexane/EtOAc 9/1→hexane/EtOAc 3/2) to give 185 mg (78% 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-53f2f2901f2e43248ea8194f1f6ed635 |
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| Source note | uspto-grants-2015_12 |
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