HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163387Generated: October 28, 2026
2-Isopropylaniline → HCID 178438961, compound
https://huagongshe.com/reaction/1163387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Isopropylaniline | HCID 12561 | — |
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | HCID 178526482 | HCID 178526482 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 178438961 | HCID 178438961 | — |
Reaction Steps
To a solution of 2-chloro-5-nitro-1H-benzimidazole (1.5 mmol; prepared from nitration of 2-chloro-1H-benzimidazole; Galy et al., J. Heterocycl. Chem. 1997, 34, 6, 1781-1788) in dry NMP (3 mL) was added 2-isopropylaniline (4 mmol). The resulting solution was subjected to microwave irradiation at 150° C. for 1 h. The contents were cooled to room temperature, diluted with water (20 mL) and extracted with EtOAc (2×15 mL). The combined extracts were then washed with water (20 mL) and brine (20 mL) and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue obtained was purified by silica gel chromatography using EtOAc/hexane as eluent to obtain (2-isopropylphenyl)-(5-nitro-1H-benzimidazol-2-yl)-amine as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820821B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-5b18bfd8daa84e858fed0b96a767900c |
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| Source note | uspto-grants-2010_10 |
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