Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 86725354 | HCID 86725354 | — |
| Product | HCID 86725353 | HCID 86725353 | — |
Reaction Steps
To a stirred solution of the product from step (a) (25 mg) in SOCl2 (1 ml) was added pyridine (1 ml). The mixture was heated to 70° C. for 30 minutes after which LCMS indicates no starting material. The volatiles were evaporated in vacuo. The residue was dissolved in EtOAc and washed with 1 M citric acid, saturated NaHCO3, brine, dried (Na2SO4), and solvent evaporated in vacuo to give the sub-titled compound (21 mg) as a colorless oil which was used as obtained in the next step. MS: ESI (positive): 330 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284277B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-3353fb7cf4dd4e8da9e012765d7b3d0b |
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| Source note | uspto-grants-2016_03 |
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