HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727415Generated: October 23, 2026
Diisopropylcarbodiimide → methyl-2-[(3,5-dimethoxyphenyl)amino]-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-1H-benzimidazole-5-carboxylate
https://huagongshe.com/en/reaction/1727415
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 3,5-Dimethoxyphenyl isothiocyanate | HCID 145422 | — |
| Reactant | Methyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoate | HCID 69027376 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl-2-[(3,5-dimethoxyphenyl)amino]-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-1H-benzimidazole-5-carboxylate | HCID 69027642 | 76% |
Reaction Steps
3,5 dimethoxyphenylisothiocyanate (571 mg, 1 eq) and diisopropylcarbodiimide (1.35 ml, 4 eq) are added successively to a solution of methyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoate (1.0 g, 1 eq) in tetrahydrofuran (10 ml). The mixture is heated under reflux for 18 hours then cooled down to ambient temperature and concentrated under reduced pressure at 40° C. The residue is taken up in ethyl acetate (100 ml) and water (40 ml). After decanting and extracting, the combined organic phases are washed with salt water, dried over Na2SO4 then evaporated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent: dichloromethane/methanol 99:1 to 98:2) produces the expected compound in the form of a beige foam (1.12 g; 76% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07495110B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-f1e39c8788fd45f9ac45d27ca0a27676 |
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| Source note | uspto-grants-2009_02 |
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