HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817248Generated: October 30, 2026
2-Aminobenzonitrile → HCID 178482916, compound
https://huagongshe.com/reaction/1817248
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminobenzonitrile | HCID 72913 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 178470770 | HCID 178470770 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178482916 | HCID 178482916 | — |
Reaction Steps
LiHMDS (3.5 eq) was added to ethyl {5-[3-(dimethylamino)pyrrolidin-1-yl]-3H-imidazo[4,5-b]pyridin-2-yl}acetate (1.0 eq) in THF at −40° C. After 10 minutes, a solution of 2-aminobenzenecarbonitrile (1.1 eq) in THF was added. The resulting mixture was allowed to warm to room temperature, stirred for 1 h and then heated to 60° C. overnight. The mixture was cooled to room temperature and quenched with NH4Cl (aq, saturated). The aqueous phase was extracted with CH2Cl2 (5 times). The product crashes out of the organic solution during the extractions. Evaporation of the solvent under reduced pressure afforded a brown solid that was triturated repeatedly with MeOH and acetone to obtain a yellow greenish powder. LC/MS m/z 390.2 (MH+), Rt 1.48 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598268B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-f3fd1cbe03a749a7a1b40990a2709f61 |
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| Source note | uspto-grants-2009_10 |
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