HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481122Generated: October 29, 2026
Dimethylformamide → HCID 22048197, compound
https://huagongshe.com/reaction/481122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 22048186 | HCID 22048186 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22048197 | HCID 22048197 | 455.1% |
Reaction Steps
A mixture of the compound obtained in Example 37 (500 mg), morpholine (99 mg), N,N-dimethylaminopyridine (13 mg), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (197 mg), and DMF (10 ml) was stirred at room temperature for 10 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4), and then evaporated under reduced pressure to remove the solvent. The residue was subjected to column chromatography on silica gel to obtain 1-{[3-chloro-4-(4-methoxyphenyl)-7-[(4-morpholinyl)carbonyl]-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-2-yl]methyl}-2,5-pyrrolidinedione (2.6 g, 92%) from the eluates with ethyl acetate. It was recrystallized from chloroform-hexane. Colorless prisms. Melting point 170-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06653476B2 |
|---|
| Source dataset | uspto-grants-2003_11 |
|---|
| ORD ID | ord-8e57e6f91481404b862a1525f235c2bc |
|---|
| Source note | uspto-grants-2003_11 |
|---|