HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068027Generated: November 2, 2026
4-Chlorobenzylamine → HCID 178522858, compound
https://huagongshe.com/reaction/1068027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | HCID 178469521 | HCID 178469521 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178522858 | HCID 178522858 | — |
Reaction Steps
A solution of ethyl 4-hydroxy-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxylate (0.315 g) from Preparation No. 51 and 4-chlorobenzylamine (0.61 nL) is heated to 180° C. for 1 h. The reaction mixture is cooled to 65° C. and diluted with CH2Cl2. Hexanes are added to initiate precipitation of the product. The resulting solid is collected and dried to yield 0.33 g of N-(4-chlorobenzyl)-4-hydroxy-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxamide as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06248739B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-8fff3fa153414afb85c0946f1519044f |
|---|
| Source note | uspto-grants-2001_06 |
|---|