HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883926Generated: October 26, 2026
Tetrahydrofuran → N-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamide
https://huagongshe.com/reaction/1883926
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Amino-5-chlorobenzonitrile | HCID 80019 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Ethyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetate | HCID 12988786 | — |
| Product | N-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamide | HCID 22664809 | — |
Reaction Steps
LiHMDS (2.5 eq) was added to ethyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetate (1.0 eq) in THF at −78° C. After 1 hour, 2-amino-5-chlorobenzenecarbonitrile (0.82 eq) in THF was added. The reaction was allowed to warm to 23° C. and stirred overnight. The resulting mixture was quenched with NH4Cl (aqueous saturated solution) and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried over Na2SO4, filtered and concentrated in vacuo to yield a brown solid. The crude material was purified by silica gel chromatography (5:1 EtOAc:hexane) to give the desired product. LC/MS m/z 396.1 (MH+), Rt 1.79 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06762194B2 |
|---|
| Source dataset | uspto-grants-2004_07 |
|---|
| ORD ID | ord-ee75b53d91664d5d938cc736289afa5f |
|---|
| Source note | uspto-grants-2004_07 |
|---|