HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Formylbenzoic acid → HCID 59340335, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | Biphenyl-2-ylcarbamic acid 1-(2-aminoethyl)piperidin-4-yl ester | HCID 53319786 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59340335 | HCID 59340335 | 92.2% |
Reaction Steps
A mixture of 4-carboxybenzaldehyde (0.95 g, 6.35 mmol) and HATU (3.02 g, 7.94 mmol) in 55 mL of DCM was stirred at room temperature for 1 hour and then biphenyl-2-ylcarbamic acid 1-(2-aminoethyl)piperidin-4-yl ester (3 g, 5.29 mmol; prepared as described in Preparation 7) and DIPEA (4.6 mL, 26.45 mmol) were added. The resulting mixture was stirred at room temperature for 2 hours and then diluted with 100 mL of DCM and washed with saturated sodium bicarbonate (150 mL) and brine (150 mL). The organic layer was dried over MgSO4, filtered and concentrated to provide 2.3 g of the title intermediate (92% yield), which was suitable for use without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728144B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-80aa58dd0d9b402ebe4d56603735b1eb |
| Source note | uspto-grants-2010_06 |