HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N3-[amino(imino)methyl]-N3-methyl-N-[4-(triphenylphosphonio)butyl]-beta-alaninamide bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Pyrazole-1-carboxamidine monohydrochloride | HCID 2734672 | — |
| Reactant | N3-methyl-N-[4-(triphenylphosphonio)butyl]-beta-alaninamide bromide | HCID 131737010 | — |
| Product | N3-[amino(imino)methyl]-N3-methyl-N-[4-(triphenylphosphonio)butyl]-beta-alaninamide bromide | HCID 131737012 | — |
Reaction Steps
N3-methyl-N-[4-(triphenylphosphonio)butyl]-β-alaninamide bromide (980 mg, 2.0 mmol) was dissolved in N,N-dimethylformamide (2 mL). The resultant solution was treated with 1H-pyrazole-1-carboximidamide hydrochloride (315 mg, 2.15 mmol) and N,N-diisopropylethylamine (0.39 mL, 2.26 mmol). The reaction was stirred overnight at room temperature. More 1H-pyrazole-1-carboximidamide hydrochloride and N,N-diisopropylethylamine can be added to effect further conversion. The reaction mixture in N,N-dimethylformamide was used without work-up in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434753B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-fb4e85a7232447ad8e7d394428661f39 |
| Source note | uspto-grants-2016_09 |