HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 6-aminonicotinate → HCID 44466098, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 6-aminonicotinate | HCID 737487 | — |
| Reactant | HCID 57919288 | HCID 57919288 | — |
| Product | HCID 44466098 | HCID 44466098 | 30% |
Reaction Steps
Using the method described in Example 66, 3-cyclopentyl-2-[4-(2-fluoro-phenoxy)-6-oxo-6H-pyridazin-1-yl]-propionic acid (Intermediate 43) and 6-amino-nicotinic acid methyl ester afforded 6-{3-cyclopentyl-2-[4-(2-fluoro-phenoxy)-6-oxo-6H-pyridazin-1-yl]-propionylamino}-nicotinic acid methyl ester as a yellow solid (200 mg, 30%); ESI-LRMS m/e calcd for C25H25F N4O5 [M+] 481, found 481 [M+H+]. 1H-NMR (300 MHz, DMSO-d6) δ ppm 1.00-1.21 (m, 1H) 1.26-1.84 (m, 8H) 1.87-2.05 (m, 1H) 2.22-2.40 (m, 1H) 3.86 (s, 3H) 5.58 (dd, J=10.9, 4.2 Hz, 1H) 5.82 (d, J=2.8 Hz, 1H) 7.29-7.56 (m, 4H) 8.10 (d, J=9.0 Hz, 1H) 8.24 (d, J=2.8 Hz, 1H) 8.28 (dd, J=9.0, 2.3 Hz, 1H) 8.87 (d, J=2.3 Hz, 1H) 11.42 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258134B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-5f46b7805f3c43cab9700d2b1add52b0 |
| Source note | uspto-grants-2012_09 |