HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Methanesulfonyl)pyrimidine → HCID 11335536, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Methanesulfonyl)pyrimidine | HCID 13289225 | — |
| Reactant | 6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amine | HCID 17743497 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11335536 | HCID 11335536 | 12% |
Reaction Steps
A solution of 6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amine (50 mg, 0.23 mmol) and 2-methylsulfonylpyrimidine (69 mg, 0.44 mmol) in N,N-dimethylformamide (0.50 mL) was heated at 150° C. for 900 seconds in a Smith Synthesizer microwave. The mixture was diluted with ethyl acetate and extracted with 5% aqueous lithium chloride. The organic layer was isolated and concentrated onto silica. Purification by flash chromatography (0-30% ethyl acetate-hexanes) yielded 6-chloro-N-pyrimidin-2-yl-2,3,4,9-tetrahydro-1H-carbazol-1-amine (8 mg, 12% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351733B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-e3342028d8f54e9593dc712b6d6ae4ab |
| Source note | uspto-grants-2008_04 |