HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710017Generated: October 30, 2026
2,2-Dimethylbutyryl chloride → HCID 71234016, compound
https://huagongshe.com/reaction/710017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethylbutyryl chloride | HCID 79958 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 71234014 | HCID 71234014 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71234016 | HCID 71234016 | — |
Reaction Steps
Furan-2-carboxylic acid [5-{2-[(2,2-dimethyl-butyryl)-methyl-amino]-ethylcarbamoyl}-2-(4-o-tolyl-piperazin-1-yl)-phenyl]-amide (compound no. 133) was prepared as follows: To a solution of furan-2-carboxylic acid [5-(2-methylamino-ethylcarbamoyl)-2-(4-o-tolyl-piperazin-1-yl)-phenyl]-amide (0.04 g, 0.086 mmol) and diisopropylethylamine (0.5 mL) in CH2Cl2 (2.0 mL), 2,2-dimethyl butyryl chloride (0.173 mmol) was added at 0° C., and the reaction was stirred at 0-25° C. for 4 h. Reaction was diluted with CH2Cl2 and washed with a solution of saturated NaHCO3. Organic layer was concentrated and dissolved in ACN and purified on preparative HPLC using water/MeOH (0.1% TFA) as eluent to give the product (0.01 g, 21% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181226B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-e0fc392b2a7b449898408c3f3dc0ade6 |
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| Source note | uspto-grants-2015_11 |
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