Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maltol | HCID 8369 | — |
| Reactant | 4,5-Dichloro-2-(tetrahydro-pyran-2-yl)-2H-pyridazin-3-one | HCID 10729262 | — |
| Reactant | Methyl 2-bromo-3-cyclopentylpropanoate | HCID 57919172 | — |
| Product | HCID 57919191 | HCID 57919191 | — |
Reaction Steps
In an analogous manner to the stepwise sequence outlined in intermediate 19, starting from 4,5-dichloro-2-(tetrahydropyran-2-yl)-2H-pyridazin-3-one (Intermediate 20) and 3-hydroxy-2-methyl-pyran-4-one and alkylating with 2-bromo-3-cyclopentyl-propionic acid methyl ester (Intermediate 10) afforded 3-cyclopentyl-2-[4-(2-methyl-4-oxo-4H-pyran-3-yloxy)-6-oxo-6H-pyridazin-1-yl]-propionic acid as a white solid (3.4 g, 30% for the final step); LC-MS: 361.1 [M+1]+ tR=3.10 min. Purity on HPLC: 97.7% (214 nm), 99.0% (254 nm), tR=5.79 min. 1H NMR (300 MHz, CDCl3): δ 7.97 (s, 1H), 7.86 (d, 1H, J=5.4 Hz), 6.59 (d, 1H, J=5.4 Hz), 6.15 (s, 1H), 5.57 (dd, 1H, J1=10.5 Hz, J2=4.5 Hz), 2.42 (s, 3H), 2.36˜2.23 (m, 1H), 2.23˜2.16 (m, 1H), 1.81˜1.57 (m, 7H), 1.32˜1.20 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08258134B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-96b7d10d4daa40cea7183a7ebd2acc9b |
|---|
| Source note | uspto-grants-2012_09 |
|---|