HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(6-Amino-1,3-benzodioxol-5-yl)ethan-1-one → N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4, 5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(6-Amino-1,3-benzodioxol-5-yl)ethan-1-one | HCID 120000 | — |
| Reactant | 2-Amino-4,5-dimethoxybenzonitrile | HCID 735967 | — |
| Reactant | N-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamide | HCID 10696210 | — |
| Product | N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4, 5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamide | HCID 9956918 | — |
Reaction Steps
N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(2-cyano-4,5-dimethoxyphenyl)aminocarbonyl]thiophene-3-sulfonamide was prepared by the method set forth for N-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamide (EXAMPLE 148) except that 2-amino-4,5-dimethoxybenzonitrile was used in stead of 2′-amino-4′,5′-(methylenedioxy)acetophenone. N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4,5-dimethoxyphenyl)aminocarbonyl]thiophene-3-sulfonamide was obtained via HPLC purification as a light brown powder (36% yield, m.p. 53-56° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06342610B2 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-8698ec224c8b4077ac05557466b9f7fb |
| Source note | uspto-grants-2002_01 |