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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351618Generated: October 27, 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/351618

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 numberUS06743791B2
Source datasetuspto-grants-2004_06
ORD IDord-bbd925ebf9f243ea9c0c131e3748fb7b
Source noteuspto-grants-2004_06