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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481082Generated: October 27, 2026

Formamidine acetate → HCID 20605616, compound

https://huagongshe.com/reaction/481082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
Reactant5-acetyl-4-oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl esterHCID 20605654—
SolventEthanolHCID 702—
ProductHCID 20605616HCID 2060561636%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a sealed tube are 5-acetyl-4-oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (1.1 mmol) and formamidine acetate (5.5 mmol) and 10 mL EtOH. The mixture is heated at 120° C. for 48 hours. The solvent is evaporated in vacuo and the residue is taken up in CH2Cl2 and washed two times with NaHCO3 (aq). The organic layer is dried over Na2SO4 and evaporated in vacuo and the residue chromatographed using 10% MeOH in CH2Cl2 as mobile phase to yield 7-Methyl-3,4,5,6-tetrahydro-3,8,10-triaza-benzo[e]azulene-1-carboxylic acid ethyl ester (36%). LRMS 271.1 found (M+1) 272

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653471B2
Source datasetuspto-grants-2003_11
ORD IDord-965bf5762c554a3d8257cb9b0f375ded
Source noteuspto-grants-2003_11