HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N'-(2-bromophenyl)sulfonyl-N,N-dimethylmethanimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | 2-Bromobenzenesulfonamide | HCID 2801263 | — |
| Solvent | Water | HCID 962 | — |
| Product | N'-(2-bromophenyl)sulfonyl-N,N-dimethylmethanimidamide | HCID 11779014 | — |
Reaction Steps
The starting material, 2-bromobenzene-1-sulfonamide, is commercially available. Reaction of 2-bromobenzene-1-sulfonamide in a solvent such as DMF, with 1,1-dimethoxy-N,N-dimethylmethanamine, followed by the addition of sodium hydrogen sulfate in water, yields 2-bromo-N-[1-dimethylaminometh-(E)-ylidene]benzenesulfonamide. This compound is reacted with 4-methylphenylboronic acid to yield 4′-methylbiphenyl-2-sulfonic acid 1-dimethylaminometh-(E)-ylideneamide, then the —(CH2)r-L moiety is added, for example, by a halogenation reaction, to form compound (1b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863309B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-0371e510ca194f56b5d72a62ea4b1cb1 |
| Source note | uspto-grants-2011_01 |