HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064194Generated: November 2, 2026
Diisopropylethylamine → HCID 69127906, compound
https://huagongshe.com/reaction/2064194
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | 4-Fluoro-2-methyl-5-nitrobenzonitrile | HCID 57345887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69127906 | HCID 69127906 | 110% |
Reaction Steps
A solution of 4-fluoro-2-methyl-5-nitrobenzonitrile (D90) (3 mmol, 540.3 mg) in dimethylformamide (20 mL) was treated with 1,1-dimethylethyl 4-amino-1-piperidinecarboxylate (3 mmol, 600.9 mg, 1 eq) and diisopropylethylamine (3 mmol, 387.6 mg, 1 eq) under argon at room temperature and then heated at 80° C. overnight. The mixture was then concentrated under reduced pressure then treated with 10% aqueous sodium carbonate solution and extracted with ether/ethyl acetate. The organics were dried and concentrated under reduced pressure to give the title compound as a solid (3.3 mmol, 1.19 mg, >100% yield). M+H 304.97 for main fragment (loss of tert-butyl group).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08288412B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-7a9ebbb0ade3447d8b27e657867df41a |
|---|
| Source note | uspto-grants-2012_10 |
|---|