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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381433Generated: November 1, 2026

3-cyclopentyl-2-[6-oxo-4-(2-pyrrolidin-1-yl-phenoxy)-6H-pyridazin-1-yl]propionic acid → HCID 44463245, compound

https://huagongshe.com/reaction/2381433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-cyclopentyl-2-[6-oxo-4-(2-pyrrolidin-1-yl-phenoxy)-6H-pyridazin-1-yl]propionic acidHCID 57919183—
Reactant1-(3-amino-1H-pyrazol-1-yl)-2-methylpropan-2-olHCID 59344938—
ProductHCID 44463245HCID 4446324534%

Reaction Steps

Using the method described in Example 17, 3-cyclopentyl-2-[6-oxo-4-(2-pyrrolidin-1-yl-phenoxy)-6H-pyridazin-1-yl]-propionic acid (Intermediate 51) and 1-(3-amino-pyrazol-1-yl)-2-methyl-propan-2-ol (Intermediate 1) afforded 3-cyclopentyl-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-2-[6-oxo-4-(2-pyrrolidin-1-yl-phenoxy)-6H-pyridazin-1-yl]-propionamide as a yellow solid (0.50 g, 34%); ES+-HRMS m/e calcd for C29H38N6O4 [M+H+] 535.3028 found 535.3027. 1H-NMR (400 MHz, DMSO-d6) δ ppm 1.05 (s, 3H), 1.06 (s, 3H), 1.08 (m, 1H), 1.25-1.73 (m, 8H), 1.83 (m, 4H), 1.93 (m, 1H), 2.25 (m, 1H), 3.22 (m, 4H), 3.89 (s, 2H), 4.67 (s, 1H), 5.44 (dd, J=4.5, J=10.7 Hz, 1H), 5.54 (d, J=2.9 Hz, 1H), 6.39 (d, J=2.3 Hz, 1H), 6.79 (m, 1H), 6.89 (dd, Jo=8.3 Hz, Jm=1.1 Hz, 1H), 7.09 (dd, Jo=7.9 Hz, Jm=1.5 Hz, 1H), 7.19 (m, 1H), 7.52 (d, J=2.3 Hz, 1H), 8.12 (d, J=2.9 Hz, 1H), 10.80 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258134B2
Source datasetuspto-grants-2012_09
ORD IDord-18856e87db6f4f39b697554efb988e0a
Source noteuspto-grants-2012_09