HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620270Generated: October 27, 2026
Sodium Iodide → 4-Amino-2-(2-butanon-3-yl)oxy-5-chloro-N-[2-(dimethylamino)-ethyl]benzamide
https://huagongshe.com/reaction/620270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Butanone, 3-bromo- | HCID 13142 | — |
| Reactant | 4-Amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-hydroxybenzamide | HCID 14372582 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Amino-2-(2-butanon-3-yl)oxy-5-chloro-N-[2-(dimethylamino)-ethyl]benzamide | HCID 14372556 | 76.6% |
Reaction Steps
A solution of 4-amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-hydroxybenzamide (1.90 g, 7.37 mmole) (prepared in Example 17), potassium carbonate (3.06 g, 2.21 mmoles), sodium iodide (1.11 g, 7.37 mmoles) and 91% 3-bromo-2-butanone (1.81 g, 12 mmoles) in DMF (30 ml) was stirred for 1.5 hours. The solvent was removed in vacuo and the residue partitioned between water and methylene chloride. The aqueous phase was extracted two more times with methylene chloride. The combined extracts were dried and concentrated in vacuo. The residue was chromatographed on a silicia gel column using the solvent system of methylene chloride (99.5)-methanol (0.5)-ammonia (0.2). The appropriate fractions were combined and concentrated in vacuo to give a solid. This was recrystallized from acetonitrile to give 1.85 g of the title compound as a colorless solid, mp. 124°-125°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04820715 |
|---|
| Source dataset | uspto-grants-1989_04 |
|---|
| ORD ID | ord-5085298142924d668dce67a2eda93218 |
|---|
| Source note | uspto-grants-1989_04 |
|---|