HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241801Generated: October 30, 2026
Triethylamine → Methyl 4-(4-(3-(6-methylpyridin-3-yl)ureido)-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/241801
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Isocyanato-2-methylpyridine | HCID 7330505 | — |
| Reactant | methyl 4-(4-amino-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate | HCID 59302728 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(4-(3-(6-methylpyridin-3-yl)ureido)-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate | HCID 11560576 | 51.1% |
Reaction Steps
To a room temperature solution of Methyl 4-(4-amino-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate (175 mg, 0.635 mmol, 1.0 equiv) and triethylamine (90 μL, 0.635 mmol, 1.0 equiv) in dry DCM (1.7 mL) was added freshly filtered 2-methyl-5-isocyanatopyridine (94 mg, 0.699 mmol, 1.1 equiv) in dry DCM (1.7 mL) dropwise via cannula. After 1 h, the reaction was diluted with DCM and washed with water and with brine. The resulting solution was dried over sodium sulfate, filtered, and concentrated in vacuo. The solid was dissolved in a minimal volume of DMF and water was added to precipitate the product. The resulting solid was filtered, washed three times with water and twice with hexane to provide the title compound as a light brown solid (133 mg, 51%). LCMS [M+H]+=410.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653081B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-076df6573c714e2f8257cf5440d5329f |
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| Source note | uspto-grants-2014_02 |
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