HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422877Generated: November 1, 2026
Azobisisobutyronitrile → HCID 71534515, compound
https://huagongshe.com/reaction/1422877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 86726296 | HCID 86726296 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 71534515 | HCID 71534515 | 53% |
Reaction Steps
To a stirred solution of (R)-6-oxo-piperidine-2-carboxylic acid ((S)-1-phenylcarbamoyl-hex-5-enyl)-amide (220 mg, 0.64 mmol), thioacetic acid (460 μl, 6.4 mmol) at 75° C. in degassed dioxane (7 ml) was added AIBN (105 mg, 0.64 mmol). The reaction mixture was stirred until complete conversion of the starting material as monitored by TLC analysis. The reaction mixture was cooled to 0° C. and quenched with an excess of cyclohexene under stirring, the latter being maintained for 20 minutes. Concentration under reduced pressure and purification through chromatography on silica gel using Hexane/DCM/IPA: 50/40/10 as eluent afforded the desired adduct.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927533B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-6628346ab84740ee9ef60fbb44c3b619 |
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| Source note | uspto-grants-2015_01 |
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