HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448064Generated: October 30, 2026
1-Naphthoic acid → HCID 69165604, compound
https://huagongshe.com/reaction/448064
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Naphthoic acid | HCID 6847 | — |
| 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 | 3-Butyl-2,5-dimethyl-1,3,4-thiadiazol-3-ium iodide | HCID 69187917 | — |
| Product | HCID 69165604 | HCID 69165604 | — |
Reaction Steps
In a 20 mL vial 1-naphthoic acid (0.9 mL of 0.2 M in DMA, 1.10 equiv) was added followed by the addition of HATU (76 mg in 0.7 mL of DMA, 0.2 mmol, 1.20 equiv.), DIEA (51 mg in 0.7 mL of DMA, 0.4 mmol, 2.40 equiv.), and finally 3-butyl-2,5-dimethyl-1,3,4-thiadiazol-3-ium iodide (49 mg in 0.7 mL of DMA, 0.17 mmol, 1 equiv.). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.87-0.93 (m, 3 H) 1.27-1.35 (m, 2 H) 1.69-1.78 (m, 2 H) 2.51 (s, 3 H) 4.16-4.20 (m, 2 H) 6.40 (s, 1 H) 7.49-7.59 (m, 3 H) 7.73-7.78 (m, 1 H) 7.94-8.01 (m, 2 H) 8.37-8.43 (m, 1 H); MS (ESI) m/z 325 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08481574B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-31727354e2654dac88be34e1677ec0c2 |
|---|
| Source note | uspto-grants-2013_07 |
|---|