HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481082Generated: October 27, 2026
Formamidine acetate → HCID 20605616, compound
https://huagongshe.com/reaction/481082
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | 5-acetyl-4-oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester | HCID 20605654 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20605616 | HCID 20605616 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653471B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-965bf5762c554a3d8257cb9b0f375ded |
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| Source note | uspto-grants-2003_11 |
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