HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620880Generated: October 27, 2026
Triethylamine → 4-{[4-(Methylthio)-1,3-thiazol-2-yl]carbamoyl}phenyl acetate
https://huagongshe.com/reaction/1620880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Acetoxybenzoyl chloride | HCID 2756254 | — |
| Reactant | 4-(Methylthio)-1,3-thiazol-2-amine | HCID 55285798 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-{[4-(Methylthio)-1,3-thiazol-2-yl]carbamoyl}phenyl acetate | HCID 57571887 | 109% |
Reaction Steps
Into a solution of 510 (0.815 g, 4.10 mmol) and dry THF (20.0 mL) was added a solution of triethylamine (0.572 mL, 4.10 mmol) and dry THF (5.00 mL), followed by a solution of 508 (0.500 g, 3.42 mmol) dissolved in dry THF (15.0 mL). The reaction was stirred at room temperature. After stirring overnight, the reaction was concentrated in vacuo. The residue was partitioned between a saturated aqueous sodium bicarbonate and dichloromethane. The dichloromethane layer was washed a second time with the saturated sodium bicarbonate solution and than twice with aq. 1 M HCl. The dichloromethane layer was dried over anhydrous magnesium sulfate and concentrated in vacuo to give crude 512 (1.15 g, >100%) as a brown solid. The crude product was suspended in diethyl ether, stirred and filtered. The filter pad was washed with ether several times, and dried in vacuo to give 512 (0.692 g, 63%) as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772502B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-e4ca9d8793a043328e2c61be81ef0ad3 |
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| Source note | uspto-grants-2014_07 |
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