HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659995Generated: October 30, 2026
tert-butyl N-(4-aminobutyl)carbamate → HCID 58945263, compound
https://huagongshe.com/reaction/659995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 58945263 | HCID 58945263 | 41% |
Reaction Steps
4,6-Dichloropyrimidine (4.14 mmol) and tert-butyl 4-aminobutylcarbamate (4.14 mmol) were dissolved in 13 ml of 2-propanol, and 3 drops of 3M aq. HCl were added. The mixture was heated in a Personal Chemistry Optimizer microwave system at 100° C. for 900 s. The reaction mixture was diluted with sat. aq. NH4Cl-solution (50 ml) and extracted with EtOAc (2×). Drying of the organic layer (Na2SO4) and evaporation of the solvent under reduced pressure yielded the crude product, which was taken up in DMSO (2.5 ml) and purified via prep.-HPLC (XTerra Prep. MS C18 5 μm, 19×150 mm, gradient from water to MeCN over 14 min), yielding 41% of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08084457B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-edd0176435804b50b5d1681e3af363bb |
|---|
| Source note | uspto-grants-2011_12 |
|---|