HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202078Generated: October 31, 2026
2-Methylquinoline-6-carboxylic acid → (S)-N-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropyl)-2-methylquinoline-6-carboxamide
https://huagongshe.com/reaction/2202078
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylquinoline-6-carboxylic acid | HCID 604483 | — |
| 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 | (S)-1-Amino-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-ol | HCID 25312355 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-N-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropyl)-2-methylquinoline-6-carboxamide | HCID 90241852 | 25% |
Reaction Steps
To a solution of 2-methylquinoline-6-carboxylic acid (1 g, 5.35 mmol) in DCM (100 mL), was added HATU (2.44 g, 6.42 mmol) and TEA (1620 mg, 16.043 mmol). The solution was stirred at 15° C. for 30 minutes before (S)-1-amino-3-(3,4-dihydro isoquinolin-2(1H)-yl)propan-2-ol (1.76 g, 8.55 mmol) was added. The resulting solution was stirred for 16 h at 15° C. until LCMS analysis showed the reaction to be complete. The mixture was then concentrated under vacuum and the residue purified by Preparative HPLC to give the desired title compound (502.1 mg, 25%). 1H NMR (400 MHz, METHANOL-d4) δ 8.31 (br. s., 1H), 8.08 (d, J=8.8 Hz, 1H), 8.12 (d, J=8.4 Hz, 1H), 7.91 (d, J=8.8 Hz, 1H), 7.47 (d, J=8.3 Hz, 1H), 7.17-7.03 (m, 4H), 4.23-4.11 (m, 1H), 3.78 (br. s., 2H), 3.59 (d, J=5.5 Hz, 2H), 2.91 (br. s., 4H), 2.78-2.69 (m, 5H). LCMS (m/z): 376.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09365519B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-989fc5176447477ca2892d9b812f98fc |
|---|
| Source note | uspto-grants-2016_06 |
|---|