HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168246Generated: October 30, 2026
N-Methyl-N-(piperidin-4-yl)benzamide → HCID 57382935, compound
https://huagongshe.com/reaction/2168246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methyl-N-(piperidin-4-yl)benzamide | HCID 12641853 | — |
| Reactant | 4-Chloro-5-methyl-7H-pyrrolo(2,3-d)pyrimidine | HCID 14809282 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57382935 | HCID 57382935 | — |
Reaction Steps
To 4-chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine D4 (0.154 g) and N-methyl-N-4-piperidinylbenzamide D15 (0.2 g) was added Ethanol (5 mL) and the reaction was heated at 150° C. for 30 minutes in the microwave. The reaction was heated again at 150° C. for 20 minutes. During the cooling, a white precipitate formed. This precipitate was filtered off and washed with Ethanol before being dried in vacuo at 40° C. to afford product in 49 mg. The filtrate was removed in vacuo and the crude residue purified by MDAP using the formic acid method. Fractions corresponding to the desired product were combined and solvent removed to give the product E32 in 22 mg. LCMS [M+H][email protected] min (2 min run)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045485B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-b826695ba6424ccd9e725ad8299be6a5 |
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| Source note | uspto-grants-2015_06 |
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