Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 69255535 | HCID 69255535 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131725870 | HCID 131725870 | 88.6% |
Reaction Steps
A mixture of intermediate (2-a) (0.023 mol) and triethylamine (0.046 mol) in DCM (40 ml) was stirred at 0° C. A mixure of methanesulfonyl chloride (0.035 mol) in DCM (10 ml) was added dropwise. The mixture was stirred on an ice bath for 2 hours and then washed with H2O/NaCl. The organic layer was dried, filtered and the solvent was evaporated. The residue (oil) was solidified in DIPE. The precipitate was filtered off and dried, yielding 5 g of (S)-2,3-dihydro-1,4-dioxino[2,3-b]pyridine-3-methanol methanesulfonate (ester) (intermediate 3) ([α]D−27.89°; c=25.10 mg/5 ml in methanol; mp. 136° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07081453B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-13068739581c41bd9f653f3721546bda |
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| Source note | uspto-grants-2006_07 |
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