Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 16225761 | HCID 16225761 | — |
| Product | HCID 58869148 | HCID 58869148 | — |
Reaction Steps
To a solution of [(R)-7-(3-fluoro-benzenesulfonyl)-chroman-2-ylmethyl]-methyl-amine (0.08 g, 0.2.8 mmol) in dry DMF (2 mL) was added triethylamine (0.1 mL, 0.72 mmol) and 3-bromoacetamide (0.32 g, 0.24 mmol). The reaction mixture was stirred for six hours at 60° C., then cooled and quenched by addition of water. The reaction mixture was extracted with diethyl ether, and the combined organic layers were washed with water and brine, dried (MgSO4), filtered and contrated under reduced pressure. Purification of the residue by flash chromatography (MeOH/methylene chloride 1/4) gave 0.08 g of 2-{[(R)-7-(3-fluoro-benzenesulfonyl)-chroman-2-ylmethyl]-methyl-amino}-acetamide as a foam. MS (M+H)=393.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754759B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-edd639813a3f405ea47097ddc3972b2a |
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| Source note | uspto-grants-2010_07 |
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