HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236716Generated: October 29, 2026
4-(Piperidin-1-ylmethyl)aniline → HCID 178486407, compound
https://huagongshe.com/reaction/2236716
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Piperidin-1-ylmethyl)aniline | HCID 846150 | — |
| Reactant | (4E)-6-bromo-7-methoxy-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione | HCID 59300399 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178486407 | HCID 178486407 | 57% |
Reaction Steps
A mixture of (4E)-6-bromo-7-methoxy-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (156 mg, 0.50 mmole), N,N-dimethylformamide (1 mL) and 4-piperidin-1-ylmethyl-phenylamine (95 mg, 0.50 mmole) is stirred and heated at 110° C. for one hour, cooled in the refrigerator. The reaction mixture is evaporated to dryness, taken up in 5% methanol in chloroform and passed through a short pad of Florisil eluting with 5% methanol in chloroform. The eluate is evaporated in vacuo, treated with acetonitrile, filtered and dried to give a dull yellow solid 134 mg (57%), mp 264-7° C.; MS (ESI): m/z 470.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713994B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-688eb637c8ab450099b4d58e117015af |
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| Source note | uspto-grants-2010_05 |
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