HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378871Generated: October 31, 2026
Hydrochloric Acid → methyl alpha-(4-(N-methylcarbamyl)aminosulfonyl-2-n-propylphenoxy)-3,4-methylenedioxyphenylacetate
https://huagongshe.com/reaction/1378871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | Methyl alpha-(2-n-propyl-4-aminosulfonyl-phenoxy)-3,4-methylenedioxyphenylacetate | HCID 19080400 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | methyl alpha-(4-(N-methylcarbamyl)aminosulfonyl-2-n-propylphenoxy)-3,4-methylenedioxyphenylacetate | HCID 53963621 | 100% |
Reaction Steps
To a stirred solution of 500 mg (1.23 mmol) of methyl α-(4-aminosulfonyl-2-n-propylphenoxy)-3,4-methylenedioxyphenylacetate (the product of Example 100, Step C) in dry dimethylformamide (2 mL) was added 80 μL (1.35 mmol) of methyl isocyanate followed by 6 mg (0.06 mmol) of cuprous chloride. The reaction mixture was stirred overnight, after which TLC analysis (5% methanol/methylene chloride) indicated the reaction had not proceeded to completion. Subsequently, an additional 80 μL (1.35 mmol) of methyl isocyanate, 6 mg (0.06 mmol) of cuprous chloride as well as 342 μL (2.46 mmol) of triethylamine was added and the reaction mixture was again stirred overnight. TLC analysis (5% methanol/methylene chloride) indicated the reaction had proceeded to completion. The reaction mixture was poured into 1N HCl and extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, filtered and the filtrate concentrated in vacuo and dried to afford 570 mg (100%) of the title compound as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668176 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-41b1c17ea1b04ca4aa1e85338a3a1b1d |
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| Source note | uspto-grants-1997_09 |
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