HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505800Generated: October 31, 2026
Diisopropylethylamine → HCID 71267450, compound
https://huagongshe.com/reaction/1505800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Azetidine hydrochloride | HCID 12308726 | — |
| Reactant | HCID 71267437 | HCID 71267437 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 71267450 | HCID 71267450 | 32.4% |
Reaction Steps
A solution of 2-chloro-N-(3-chloro-2-methylphenyl)-6-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-1H-benzimidazole-4-carboxamide (80 mg, Example 135), azetidine hydrochloride (60 mg) and N,N-diisopropylethylamine (208 μL) in EtOH (1.8 mL) was reacted at 120° C. for 20 minutes in a microwave reactor (Biotage, Initiator). The reaction mixture was concentrated under reduced pressure, and the residue was purified on column chromatography to obtain 2-(azetidin-1-yl)-N-(3-chloro-2-methylphenyl)-6-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-1H-benzimidazole-4-carboxamide (27 mg). This was dissolved in MeOH (1 mL), 2N hydrogen chloride/MeOH solution (1 Eq) was added, and it was stirred and concentrated. The residue was triturated in diethyl ether, and the precipitate was collected by filtration and dried to obtain the titled compound (21 mg) as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216968B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-c3d87b1decac41a986bd123c33361205 |
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| Source note | uspto-grants-2015_12 |
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