HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504044Generated: November 2, 2026
Dimethylformamide → HCID 86613953, compound
https://huagongshe.com/reaction/504044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Methylbenzaldehyde | HCID 10722 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86613954 | HCID 86613954 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86613953 | HCID 86613953 | 50.5% |
Reaction Steps
To 5-(8-methoxy-1-piperidin-4-ylmethyl-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl)thiazolidine-2,4-dione (20 μmol, 1.0 eq.) was added a DMF (200 μl) solution of 2-methylbenzaldehyde (24 μmol, 1.2 eq) and acetic acid (10 μl). Si-sodium cyanoborohydride was added further thereto. The solution was shaken for several minutes, diisopropylethylamine (30 μl) was added, and a reaction was carried out at room temperature overnight. The resin was removed by filtration and washed with dichloromethane. The solvent was distilled off from the filtrate in a nitrogen gas stream, and the residue was purified by HPLC (UV-trigger, column: CAPCELL PAK C18, UG 120 S-5, 20 mm×50 mm, 0.05% trifluoroacetic acid-H2O, 0.05% trifluoroacetic acid-CH3CN). The structure was confirmed by LC-MS, and freeze-drying was conducted, giving 5-{8-methoxy-1-[1-(2-methylbenzyl)piperidin-4-yl]methyl-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl}thiazolidine-2,4-dione in 50.5% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777038B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-8d7ff5ef21b14993bb4811e524fbb953 |
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| Source note | uspto-grants-2010_08 |
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