Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 20544697 | HCID 20544697 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20544691 | HCID 20544691 | 46.5% |
Reaction Steps
500 ml of dioxane, 50 ml of water, 49 g of 7-[(1-adamantyl)-sulfamoyl]-1,4-benzodioxane-5-carboxylic acid and 12.5 g of triethylamine were introduced into a 2-liter balloon flask provided with an agitator and a thermometer. The solution was agitated at ambient temperature and then 17 g of isobutyl chloroformiate was added. The mixture was agitated and then 10 g of butylamine was introduced. After agitation of the mixture dioxane was removed. The residue was dissolved in 200 ml of hot water. The crystals formed by cooling were washed with water, dried and redissolved in 250 ml of acetone at boiling temperature. The solution was filtered hot. The crystals formed by cooling were dried off, washed and dried. 26 g of N-(butyl)-7-[(1-adamantyl)sulfamoyl]-1,4-benzodioxane-5-carboxamide was produced (M.P. 147° C.; yield: 46.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04306072 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-cf63c060d09e447c9285b9de1d401176 |
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| Source note | uspto-grants-1981_12 |
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