HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703532Generated: October 30, 2026
Triethylamine → N-[4-[2-(Dimethylamino)ethoxy]benzyl]-5-dimethylaminosulfonyl 2-methoxybenzamide
https://huagongshe.com/reaction/703532
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | p-(2-(Dimethylamino)ethoxy)benzylamine | HCID 88349 | — |
| Reactant | 5-(N,N-dimethylsulfamoyl)-2-methoxybenzoic acid | HCID 13576895 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-[2-(Dimethylamino)ethoxy]benzyl]-5-dimethylaminosulfonyl 2-methoxybenzamide | HCID 15622788 | 91.4% |
Reaction Steps
To a cooled suspension of 3.20 g of 5-dimethylaminosulfonyl-2-methoxybenzoic acid in 10 ml of tetrahydrofuran were successively added dropwise 1.25 g of triethylamine and 1.34 g of ethyl chloroformate with stirring. The mixture was stirred at the same temperature for 30 minutes and then a solution of 2.00 g of 4-[2-(dimethylamino)ethoxy]benzylamine in 10 ml of tetrahydrofuran was added dropwise with stirring. The mixture was stirred at room temperature for 2 hours and the solvent was evaporated. Hydrochloric acid (10%) was added to the residue and the aqueous solution was washed with ethyl acetate. The aqueous layer was made alkaline with potassium carbonate and was extracted with ethyl acetate. The extract was dried and evaporated. The residue was washed with isopropyl ether to give 4.10 g of colorless crystals, which were recrystallized from a mixture of ethyl acetate and ether to give colorless needles, m.p. 99.5°-100.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983633 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-0998027b0f7c46eb9408bc62bd472629 |
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| Source note | uspto-grants-1991_01 |
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