HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 67274399, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 67274196 | HCID 67274196 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67274399 | HCID 67274399 | 82.3% |
Reaction Steps
To a solution of 0.198 g 6-amino-4-methylsulfanyl-pyridine-2-carboxylic acid methyl ester in 4 ml tetrahydrofuran was added 0.044 g lithiumborohydride and the mixture was stirred at room temperature for 3 h. The reaction mixture was partitioned between ethyl acetate and brine. The phases were separated and the organic phase was purified by chromatography on silica gel with ethyl acetate to ethyl acetate:methanol=9:1. to yield 0.14 g of the title compound as beige crystals. MS (ISP): 171.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163778B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-d4af3558c7a340ca82b531cdd57d0aa1 |
| Source note | uspto-grants-2012_04 |