Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912906Generated: October 30, 2026

(2-Hydroxyphenyl)acetic acid → N-[3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-2-yl]-2-(2-hydroxyphenyl)acetamide

https://huagongshe.com/reaction/1912906

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Hydroxyphenyl)acetic acidHCID 11970—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-(4-Chlorophenyl)pyrazolo[1,5-a]pyrimidin-2-amineHCID 68751295—
SolventPyridineHCID 1049—
ProductN-[3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-2-yl]-2-(2-hydroxyphenyl)acetamideHCID 6875119519.3%

Reaction Conditions

Temperature35 °C

Reaction Steps

The product from Example 99A (100 mg, 0.41 mmol), 2-hydroxyphenylacetic acid (124 mg, 0.82 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (157 mg, 0.82 mmol), 1-hydroxybenzotriazole hydrate (100 mg, 0.65 mmol) were combined with pyridine (8 mL) and stirred at 35° C. for 18 hours. The reaction mixture was concentrated under vacuum and purified by reverse-phase HPLC [Waters XBridge™ RP18 column, 5 μm, 30×100 mm, flow rate 40 mL/minute, 5-95% gradient of acetonitrile in buffer (0.1 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to afford 30 mg (19%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 10.28-10.56 (bs, 1H), 9.09 (dd, J=6.9, 1.7 Hz, 1H), 8.62 (dd, J=4.1, 1.7 Hz, 1H), 7.70-7.73 (m, 2H), 7.30-7.34 (m, 2H), 7.11-7.16 (m, 2H), 6.72-6.81 (m, 2H), 6.65-6.72 (m, 1H), 3.57 (s, 2H); MS (ESI) m/z 379 (M+H)+; Anal. calculated for C20H15ClN4O2.0.35H2O: C, 62.37; H, 4.11; N, 14.55. Found C, 62.16; H, 3.87; N, 14.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609669B2
Source datasetuspto-grants-2013_12
ORD IDord-dac0b7bb391843e7b2733810a4777214
Source noteuspto-grants-2013_12