HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409754Generated: October 30, 2026
HCID 86686154, compound → HCID 86686161, compound
https://huagongshe.com/reaction/1409754
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86686154 | HCID 86686154 | — |
| Reactant | HCID 178449908 | HCID 178449908 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86686161 | HCID 86686161 | — |
Reaction Steps
0.5 M solution of zinc chloride in tetrahydrofuran (4.52 mL) is added dropwise at room temperature to a mixture of N-hydroxy-isobutyramidine (58 mg) and N-(1-cyano-piperidin-4-yl)-N-cyclopropyl-6-(4-methanesulfonyl-phenyl)-nicotinamide (160 mg) in ethyl acetate (8 mL). The reaction mixture is stirred at 50° C. for two days and cooled to room temperature. The precipitate is filtered off and heated to 100° C. for 1 h in a mixture of ethanol (6 mL) and glacial acetic acid (3 mL). The solvents are evaporated in vacuo and dichloromethane and 10% aqueous K2CO3 solution are added to the residue. The organic phase is separated, washed with brine, dried over MgSO4 and concentrated in vacuo. The residue is triturated with diethyl ether to give the title compound. LC (method 8): tR=1.51 min; Mass spectrum (ESI+): m/z=510 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921398B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-54a11b82239d480db8a29a672d32cf93 |
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| Source note | uspto-grants-2014_12 |
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