Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Amino-N-methylbenzamide | HCID 676526 | — |
| Reactant | HCID 59205698 | HCID 59205698 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ammonia | HCID 222 | 2% |
| Product | HCID 59205684 | HCID 59205684 | — |
Reaction Steps
To 1-chloro-N-(isoquinolin-6-yl) methanesulfonamide in MeOH is added KI and the solution is heated to 60° C. for 40 minutes. The mixture is cooled to 45° C. and 3-amino-N-methylbenzamide is added and stirred at 45° C. After 2-4 hours or when TLC indicated completion of the reaction, the solvents are evaporated and the residue is taken up in EtOAc and extracted with NaHCO3 (sat). The organics are dried (Na2SO4), filtered and evaporated. Flash chromatography (SiO2, 2% NH3(2M) in MeOH/3% MeOH/CH2Cl2) gives 3-((N-isoquinolin-6-ylsulfamoyl)methylamino)-N-methylbenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034943B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-c8b8ce44dd6c470aabe205bb6c5af9e2 |
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| Source note | uspto-grants-2011_10 |
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