HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (R)-6-amino-4-((1-methoxypropan-2-yl)oxy)nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | (R)-1-methoxypropanol | HCID 92954563 | — |
| Reactant | 6-Amino-4-fluoronicotinonitrile | HCID 118036901 | — |
| Product | (R)-6-amino-4-((1-methoxypropan-2-yl)oxy)nicotinonitrile | HCID 118036909 | — |
Reaction Steps
A solution of KHMDS in THF (1M, 43.8 ml, 43.8 mmol) was added to a solution of (R)-1-methoxypropanol (4.3 ml, 43.8 mmol) in THF (50 ml) at room temperature under a positive argon pressure. After stirring for 15 minutes at room temperature a solution of 6-amino-4-fluoronicotinonitrile (intermediate 21, 3.0 g, 21.88 mmol) in THF (30 ml) was added drop wise. The reaction mixture was stirred for 65 h at room temperature, partitioned between aqueous NH4Cl and
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266883B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-7e50e10a9f4344a48b699d88cf1a9547 |
| Source note | uspto-grants-2016_02 |