HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515281Generated: October 29, 2026
Carbamic acid, 4-pyridinyl-, phenyl ester → 1-(4-((1-(4-(1,1,1,3,3,3-Hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea
https://huagongshe.com/reaction/515281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbamic acid, 4-pyridinyl-, phenyl ester | HCID 11401617 | — |
| Reactant | HCID 86670937 | HCID 86670937 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(4-((1-(4-(1,1,1,3,3,3-Hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea | HCID 52919057 | 26.5% |
Reaction Steps
Phenyl pyridin-4-ylcarbamate (1.680 mmol, 0.36 g) was added to a stirred solution of 2-(4-((4-(4-aminobenzyl)piperidin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (1.120 mmol, 0.5 g) in dioxane (20 mL) and the mixture heated in a microwave for 10 minutes at 130° C. followed by 5 minutes at 130° C. The mixture was washed with water (10 mL) and the organic phase dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by HPLC and concentrated under reduced pressure to afford the title compound (168 mg). MS (ESI) m/z 567.5 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09108939B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-dd75a4cf19ab4696ae56c897acbe1636 |
|---|
| Source note | uspto-grants-2015_08 |
|---|