Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| 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 | HCID 178422078 | HCID 178422078 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44199933 | HCID 44199933 | — |
Reaction Steps
To a solution of benzoic acid (0.67 g, 5.5 mmol), HATU (2.09 g, 11 mmol) and DIPEA (1.05 mL, 6 mmol) in dry DMF (10 mL) at rt in the presence of anhydrous Na2SO4 (7 g, 50 mmol) was added 17 (1.69 g, 5 mmol) slowly. The consumption of 17 was determined to be completed by LC/MS. Additional anhydrous DMF (40 mL) was added and the mixture was heated at 100° C. for 1 h. Solid was filtered off and most of DMF was removed under vacuum. The residue was partitioned between a mixture of water (150 mL), aqueous Na2CO3 (2 M, 10 mL), EtOAc (200 mL) and MeOH (20 mL). The organic phase was washed further with water (2×50 mL). After drying and removal of EtOAc, the solid residue was suspended and stirred in ACN (40 mL) for 16 h. Filtration and washing with copies amounts of ACN yielded A7 as a solid. 1H NMR (400 MHz, d4-MeOH) δ 9.03 (s, 1H), 8.12 (s, 1H), 8.1 (d, J=1.5 Hz, 1H), 8.05 (s, 1H), 7.83 (s, 1H), 7.65 (d, J=6.2 Hz, 1H), 7.59 (d, J=6.3 Hz, 1H), 7.57 (d, J=7.2 Hz, 1H), 7.5 (d, J=2.4 Hz, 1H), 7.43 (dd, J=8.3, 2.5 Hz, 1H), 7.27 (d, J=8.4 Hz, 1H), 3.84 (s, 3H), 2.83 (s, 3H), 2.18 (s, 3H). MS m/z 424.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08278452B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-2b0bdf986410460ea64649740135af3d |
|---|
| Source note | uspto-grants-2012_10 |
|---|