HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245384Generated: October 30, 2026
Isovaleryl chloride → HCID 178429853, compound
https://huagongshe.com/reaction/2245384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isovaleryl chloride | HCID 66054 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Methylene-3-(2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)thiazolidin-2-imine | HCID 86619167 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178429853 | HCID 178429853 | — |
Reaction Steps
To a solution of 5-methylene-3-(2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)thiazolidin-2-imine (Example 22C, 0.14 g, 0.44 mmol) in acetonitrile (3 mL) was added Hunig's base (0.062 g, 0.48 mmol) followed by 3-methylbutanoyl chloride (0.08 g, 0.66 mmol). The mixture was heated for 12 hours at 65° C. The reaction mixture was cooled down and more 3-methylbutanoyl chloride (0.08 g, 0.66 mmol) was added. The mixture was heated again at 65° C. for 12 hours. After cooling off, the mixture was diluted with CH2Cl2 (50 mL) and washed with water and brine. The organic phase was dried over sodium sulfate, filtered and dried. After evaporation under reduced pressure the residue was chromatographed over silica using CH2Cl2 100%-5%MeOH/CH2Cl2 to supply the titled compound. 1H NMR (CDCl3) δ ppm 0.95 (6H), 2.20 (1H), 2.35 (3H), 2.40 (2H), 6.75 (1H), 7.20 (1H), 7.30 (1H), 7.40 (1H); MS (ESI) m/z 405(M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683084B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-264b4426911d46bf8ae412360695644c |
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| Source note | uspto-grants-2010_03 |
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