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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852305Generated: October 30, 2026

4-(3-Dimethylamino-2-methoxymethyl-acryloyl)-1H-pyrrole-2-carboxylic Acid (2-hydroxy-1-(S)-phenyl-ethyl)-amide → 4-(5-Methoxymethyl-2-phenylamino-pyrimidin-4-yl)-1H-pyrrole-2-carboxylic acid (2-hydroxy-1-(S)-phenyl-ethyl)-amide

https://huagongshe.com/reaction/852305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Dimethylamino-2-methoxymethyl-acryloyl)-1H-pyrrole-2-carboxylic Acid (2-hydroxy-1-(S)-phenyl-ethyl)-amideHCID 86587976—
ReactantHCID 178418923HCID 178418923—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product4-(5-Methoxymethyl-2-phenylamino-pyrimidin-4-yl)-1H-pyrrole-2-carboxylic acid (2-hydroxy-1-(S)-phenyl-ethyl)-amideHCID 600906022.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

4-(3-Dimethylamino-2-methoxymethyl-acryloyl)-1H-pyrrole-2-carboxylic acid (2-hydroxy-1-(S)-phenyl-ethyl)-amide (0.27 mmol) was combined with phenyl guanidine (73 mg) in N,N-dimethylacetamide (2 mL) and the resulting suspension was heated at 90° C. for 35 hours. The reaction mixture was diluted with ethyl acetate, washed with saturated NaHCO3 and brine, dried over MgSO4 and concentrated in vacuo. The crude product was purified by prep HPLC (Gilson: Column=CombiHT SB-C189 5 μM, 21.2 mm×100 mm, eluent=0.1% TFA MeCN/H2O gradient) to afford III-a-164 as a yellow solid (3.2 mg). LC/MS(m/z) 444.16 (M+1), 442.19 (M−1); HPLC Method B, Rt=5.16 minutes: 1H NMR consistent with structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253187B2
Source datasetuspto-grants-2007_08
ORD IDord-825d951df1f4466fa18b8435d520021b
Source noteuspto-grants-2007_08