HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592973Generated: October 26, 2026
Tetrahydrofuran → Methyl 7-{[4'-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-ylmethyl]methylcarbamoyl}heptanoate
https://huagongshe.com/reaction/1592973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 8-chloro-8-oxooctanoate | HCID 4586585 | — |
| Reactant | 5-(3'-Methylaminomethylbiphenyl-4-ylmethyl)thiazolidine-2,4-dione | HCID 12085486 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 7-{[4'-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-ylmethyl]methylcarbamoyl}heptanoate | HCID 10345737 | — |
Reaction Steps
600 mg (1.36 mmol) of 5-(3′-methylaminomethylbiphenyl-4-ylmethyl)thiazolidine-2,4-dione, 10 ml of THF and 600 μl (4.3 mmol) of triethylamine are introduced into a round-bottomed flask and under a nitrogen stream. 220 μl (1.55 mmol) of methyl 8-chloro-8-oxooctanoate are added dropwise and the mixture is stirred for one hour. The reaction medium is poured into water, extracted with dichloromethane, the organic phase decanted off, washed with water, dried over magnesium sulphate and evaporated off. The residue obtained is purified by chromatography on a silica column eluted with a dichloromethane and ethyl acetate (80-20) mixture. After evaporation of the solvents, 350 mg (50%) of methyl 7-{[4′-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-ylmethyl]methylcarbamoyl}heptanoate are recovered in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07294639B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-8ddba5a1480c4b09b4ee4d065dc01f56 |
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| Source note | uspto-grants-2007_11 |
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