HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188584Generated: October 26, 2026
5-Isocyanato-1,3-dioxaindane → N-({1-[4-(3-Benzo[1,3]dioxol-5-yl-ureido)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamide
https://huagongshe.com/reaction/2188584
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Isocyanato-1,3-dioxaindane | HCID 5223213 | — |
| Reactant | N-{[1-(4-Amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide TFA salt | HCID 86646662 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-({1-[4-(3-Benzo[1,3]dioxol-5-yl-ureido)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamide | HCID 49763338 | — |
Reaction Steps
5-Isocyanato-benzo[1,3]dioxole (Aldrich, 50 mg, 0.302 mmol) was added into a solution of N-{[1-(4-amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide TFA salt (150 mg, 0.302 mmol) and TEA (127 μL, 0.906 mmol) in DMF (3 mL) at room temperature. The reaction was stirred overnight and quenched with saturated sodium bicarbonate. The reaction was then partitioned between DCM and water. The organic layer was separated and the aqueous layer was extracted 3 times with a chloroform/IPA “cocktail” (˜3:1, v/v). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was then purified by a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford the title compound as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324186B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-c420370e899d4d12ac1be46e9aea3e48 |
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| Source note | uspto-grants-2012_12 |
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