HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781624Generated: October 30, 2026
Triethylamine → 4-chloro-N-(methoxycarbonylmethylthio)acetylanthranilic acid methyl ester
https://huagongshe.com/reaction/1781624
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-chloroanthranilate | HCID 80001 | — |
| Reactant | Methyl [(2-chloro-2-oxoethyl)sulfanyl]acetate | HCID 12361281 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-chloro-N-(methoxycarbonylmethylthio)acetylanthranilic acid methyl ester | HCID 22364774 | — |
Reaction Steps
21.24 g (0.114 mol) of 4-chloroanthranilic acid methyl ester and 19.1 ml (0.137 mol) of triethylamine are placed in 180 ml of methylene chloride at 0°. A solution of 20.9 g (0.114 mol) of 2-(chloroformylmethylthio)-acetic acid methyl ester (T. Terasawa and T. Okada, J. Org. Chem., 42, 1163 (1977)) in 20 ml of methylene chloride is added dropwise thereto and the mixture is then stirred for 15 minutes at 0° and for 3 hours at room temperature. The reaction mixture is extracted with water and brine and the aqueous phases are washed with methylene chloride. The organic phases are combined, dried with sodium sulfate, filtered and concentrated. Chromatography of the crude product on silica gel with hexane/ethyl acetate (4:1) yields, in the form of yellowish crystals, 4-chloro-N-(methoxycarbonylmethylthio)acetylanthranilic acid methyl ester which is still impure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05633379 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-3c74e80b8099436f9d73ec980f6d944a |
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| Source note | uspto-grants-1997_05 |
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