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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350382Generated: October 31, 2026

Acetic acid ethanol → HCID 69333117, compound

https://huagongshe.com/reaction/350382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid ethanolHCID 18476134—
ReactantHCID 86587782HCID 86587782—
CatalystPalladiumHCID 23938—
ProductHCID 69333117HCID 6933311724%

Reaction Steps

A stirred mixture of 4-[4-benzyloxy-1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinylmethoxy]-3-methoxybenzoate (440 mg, 0.645 mmol) and 5% Pd/C (400 mg) in AcOH:EtOH (1:1, v/v, 100 mL) was hydrogenated at 1 atm for 5 hr. The mixture was filtered to remove the catalyst and the filtrate was concentrated in vacuo. The residue was chromatographed on silica-gel with CHCl3:EtOH (10:1, v/v) as eluent to give 90 mg (24%) ethyl 4-[4-hydroxy-1-[3-methoxy-4-[N′-(2-methylphenyl)ureido]phenylacetyl]-2-pyrrolidinylmethoxy]-3-methoxybenzoate as a pale yellow oil. 1H-NMR (CDCl3) δ 1.39 (3 H, t, J=7.3 Hz), 2.04–2.37 (total 5 H, m), 3.44–4.70 (16 H, series of m), 6.63 (1 H, s), 6.70–6.80 (2 H, m), 6.84 (1 H, d, J=8.3 Hz), 7.11 (1H, t, J=7.8 Hz), 7.20–7.24 (3 H, m), 7.45 (1 H, d, J=2.0 Hz), 7.59 (2 H,dd, J=8.3, 2.0 Hz), 8.01 (1 H, d, J=7.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-d91f6e6151f94563997c66190b4e2d4b
Source noteuspto-grants-2007_02