HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893521Generated: October 28, 2026
Dicyclohexylcarbodiimide → HCID 15022942, compound
https://huagongshe.com/reaction/893521
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 15022941 | HCID 15022941 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15022942 | HCID 15022942 | 75.2% |
Reaction Steps
A stirred solution of 0.50 g (0.0013 mole) of 2-chloro-3-[2,4-dichloro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenyl]propionic acid (Compound 2), 0.071 g (0.0013 mole) of cyclopropylamine, 0.17 g (0.0013 mole) of 1-hydroxybenzotriazole hydrate, and 0.18 g (0.0014 mole) of N,N-diisopropylethylamine in approximately 15 mL of tetrahydrofuran was cooled to 0° C. To this cold mixture was added 0.26 g (0.0013 mole) of 1,3-dicyclohexylcarbodiimide. After complete addition, the reaction mixture was allowed to warm to room temperature and was stirred for approximately 18 hours. The reaction mixture was filtered. The filtrate was diluted with carbon tetrachloride and was washed in succession with a IN hydrochloric acid solution, an aqueous 10% sodium hydroxide solution, water, and an aqueous saturated sodium chloride solution. The organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated under reduced pressure to give 0.43 g of N-cyclopropyl2 -chloro-3-[2,4-dichloro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenyl]propionamide as a solid, m.p. 139°-143° C., Compound 17 of Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05125958 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-1fbd9a5e4b284dacabcc8d7ce34fa79e |
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| Source note | uspto-grants-1992_06 |
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