HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642021Generated: October 28, 2026
Diisopropylethylamine → HCID 57831211, compound
https://huagongshe.com/reaction/1642021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-(4-Bromomethylphenyl)-2-methyl-2H-tetrazole | HCID 589329 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57831211 | HCID 57831211 | 36.9% |
Reaction Steps
A solution of 23 grams (0.091 mole) of 5-[4-(bromomethyl)phenyl]-2-methyl-1,2,3,4-tetrazole, 14 grams (0.091 mole) of 4-piperidone monohydrate hydrochloride, and 47 mL (3 equivalents) of N,N-diisopropylethylamine in 200 mL of dimethylsulfoxide (DMSO) was stirred for about 3 days. The reaction was quenched by pouring the reaction mixture onto 400 mL of dilute, cold sodium hydroxide. The resultant solution was extracted one time with 300 mL of ethyl acetate. An emulsion formed, which was broken up by warming it to about 35° C. The organic layer was separated and concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using 40:1 methylene chloride:methanol as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 9.12 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08119563B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-400147d6f459463cb9a4695ad0a6af5f |
|---|
| Source note | uspto-grants-2012_02 |
|---|