HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060592Generated: October 31, 2026
4-Chlorobenzylamine → HCID 178522927, compound
https://huagongshe.com/reaction/1060592
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | HCID 178469654 | HCID 178469654 | — |
| Product | HCID 178522927 | HCID 178522927 | 75% |
Reaction Steps
A suspension of ethyl 4-hydroxy-8-iodo-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxylate (0.8 g) and 4-chlorobenzylamine (1.54 mL) is heated to 180° C. for 1 h. The reaction is cooled to room temperature. The resulting solid is collected and washed with Et2O. The crude solid is adsorbed onto silica and chromatographed (Biotage flash 40S, eluant 1% MeOH/CH2Cl2 then 2% MeOH/CH2Cl2). Fractions homogeneous by TLC are combined and concentrated. The resulting solid is triturated with EtOAc/hexanes to yield 0.73 g (75%) of N-(4-chlorobenzyl)-4-hydroxy-8-iodo-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxamide as a white solid, m.p. 257-259° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06525049B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-6bb8d5776fcc4a70a62002b5d7a4cf36 |
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| Source note | uspto-grants-2003_02 |
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