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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292134Generated: October 30, 2026

Ammonia → HCID 19864533, compound

https://huagongshe.com/reaction/2292134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantN-tert-butyl-3-oxobutanamideHCID 257712—
ProductHCID 19864533HCID 19864533—

Reaction Steps

N-t-butyl-3-ketobutanamide (0.29 g) was dissolved in saturated ethanolic ammonia (15 ml) and stirred overnight at room temperature. The solution was evaporated to yield N-t-butyl-3-aminocrotonamide which was used directly. The crude residue was dissolved in ethanol (8 ml), 2-chlorobenzaldehyde (0.28 g) and ethyl 4-[2-(2-methylbenzimidazol-1-yl)ethoxy]-3-ketobutanoate (0.61 g) were added. The mixture was heated at reflux overnight, cooled and the solvent removed under reduced pressure. The residue was chromatographed on silica eluting with 4% diethylamine in ethyl acetate. The fractions containing the product were combined and evaporated. The residue was re-chromatographed on silica eluting with 5% methanol in ethyl acetate. The fractions containing the product were combined and evaporated to yield the title compound (0.17 g, 15%). m.p. 157°-161° C. Found: C, 65.66; H, 6.68; N, 9.74. C31H37C1N4O4 requires C, 65.89; H, 6.60; N, 9.91%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801598
Source datasetuspto-grants-1989_01
ORD IDord-a3ed0705cf354752aa7c6afb4ede0d38
Source noteuspto-grants-1989_01