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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481092Generated: October 30, 2026

Methanol → HCID 20605630, compound

https://huagongshe.com/reaction/481092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium BicarbonateHCID 516892—
ReactantPyridine-4-amidine hydrochlorideHCID 2776844—
ReactantHCID 20872400HCID 20872400—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20605630HCID 2060563053.2%

Reaction Steps

A mixture of 5-Bromo-4-oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester(467 mg, 1.2 mmol), 4-Amidinopyridine hydrochloride(953 mg, 6.1 mmol), and NaHCO3(813 mg, 9.7 mmol) in dioxane(20 mL) is refluxed for 20 h. After cooling to RT, MeOH(5 mL) is added and the mixture is filtered. The filtrate is concentrated in vacuo and the brown residue is purified by flash chromatography on silica gel (10% MeOH/CH2Cl2) to yield 197 mg of 2-Pyridin-4-yl-4,5,6,7-tetrahydro-3H-1,3,7-triaza-cyclopenta[e]azulene-9-carboxylic acid methyl ester as a yellow solid (53%). 1H NMR (CDCl3) 2.06 (quint, 2H), 2.98 (t, 2H), 3.04 (t, 2H), 3.91 (s, 1H), 7.46 (s, 1H), 7.76 (d, 2H) 8.28 (br s, 1H) 8.56 (d, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653471B2
Source datasetuspto-grants-2003_11
ORD IDord-0a903add14a84efd9b02d43b0638f3bf
Source noteuspto-grants-2003_11