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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013090Generated: October 31, 2026

Acetic Acid → HCID 44243038, compound

https://huagongshe.com/reaction/1013090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl 4,4,4-triethoxybutanoateHCID 13452377—
ReactantHCID 44243036HCID 44243036—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 44243038HCID 4424303865%

Reaction Conditions

Temperature85 °C

Reaction Steps

4-Amino-1-(2-(3-ethylureido)benzo[b]thiophene-3-carbonyl)piperidine-4-carboxamide (7, 100 mg, 1.0 equivalent) as prepared in Example 7 was dissolved in toluene (0.09 M) and DMF (0.26 M), and to which acetic acid (2.0 equivalents), and ethyl 4,4,4-triethoxybutanoate (4.0 equivalents) were added and the reaction mixture was heated to 85° C. for 9 hrs. The reaction mixture was then partitioned between ethyl acetate and water and the separated organics was washed with brine and dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by SiO2 chromatography (5%-10% MeOH/CH2Cl2 gradient) to afford ethyl 3-(8-(2-(3-ethylureido)benzo[b]thiophene-3-carbonyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-en-2-yl)propanoate (10, 65%). Two rotamers observed (ratio 1.3:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981904B2
Source datasetuspto-grants-2011_07
ORD IDord-5c8e6aa685ce424e95a19a6b0660754c
Source noteuspto-grants-2011_07