HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728382Generated: November 1, 2026
Dicyclohexylcarbodiimide → HCID 10370529, compound
https://huagongshe.com/reaction/1728382
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3-Pyridinemethanamine | HCID 31018 | — |
| Reactant | HCID 54449037 | HCID 54449037 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10370529 | HCID 10370529 | — |
Reaction Steps
100 mg of N-[(R)-1-[(1,1-dimethylethoxy)carbonyl]-3-(1,3-dihydro-1,3-dioxo-2H-benz[f]isoindol-2-yl)propyl]-L-leucine, prepared as in Example L, was added to 2.5 mL of DMF. 39.2 mg of hydroxybenzotriazol.H2O was added to the mixture followed by 0.026 mL of (pyridin-3-ylmethyl)amine. The mixture was cooled to 0° C. and 52.8 mg dicyclohexylcarbodiimide was added. The mixture was warmed to 23° C. and stirred for 24 h. The solvents were removed by evaporation and the resultant residue was diluted with ethyl acetate. The mixture was extracted with a saturated solution of sodium bicarbonate and the organic layer was separated, dried (MgSO4), and filtered. The solvent was removed by evaporation to afford the title compound; 139 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05326760 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-ea08da99fbfa42fbb81fc4f9017edad1 |
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| Source note | uspto-grants-1994_07 |
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