HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735840Generated: October 30, 2026
Diisopropylethylamine → HCID 67189229, compound
https://huagongshe.com/reaction/735840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(1-Naphthyl)ethylamine | HCID 98089 | — |
| Reactant | HCID 67187025 | HCID 67187025 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 67189229 | HCID 67189229 | — |
Reaction Steps
The resin-bound 4-chloromethyl-N-dodecyl-benzamide (described in step b, 0.0426 mmol) was swelled in NMP (0.25 mL) for 15 min at rt. DIEA (33 mg, 0.256 mmol), tetrabutyl-ammonium iodide (94.4 mg, 0.256 mmol) and 1-naphthalen-1-yl-ethylamine (44 mg, 0.256 mmol) dissolved in NMP (0.75 mL) were added and the reaction mixture was shaken 14 h at 80° C. The resin was washed successively with THF (1×15 min), MeOH (1×15 min), THF (1×15 min), MeOH (3×10 min), DMF (3×10 min), MeOH (1×5 min), THF (3×10 min), MeOH (1×5 min), DCM (3×10 min) and with Et2O (1×10 min). The resin was then dried under vacuum to afford the resin-bound N-dodecyl-4-({[1-(1-naphthyl)ethyl]amino}-methyl)benzamide which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592477B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-a09bb88c449149258ae549893e6eb62f |
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| Source note | uspto-grants-2009_09 |
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