HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-amino-3,4-dihydro-2H-1,4-benzothiazin-3-one → HCID 67222622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-amino-3,4-dihydro-2H-1,4-benzothiazin-3-one | HCID 686901 | — |
| Reactant | HCID 11217932 | HCID 11217932 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 67222622 | HCID 67222622 | 83% |
Reaction Steps
A solution of 6-amino-4H-benzo[1,4]thiazin-3-one (10.68 g, 59.3 mmol; commercial) and tert-butyl-dimethyl-((R)-2-oxiranyl-ethoxy)-silane (as described in H.i, 12.0 g, 59.3 mmol) in 9-1 EtOH/H2O (320 mL) was heated at 80° C. for 2 days. The mixture was concentrated under reduced pressure. Residual starting aniline could be removed by addition of ether/MeOH followed by filtration. The mother liquor containing the product was concentrated under reduced pressure to afford the title intermediate as a brown oil (18.8 g, 83% yield) which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349826B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-88362eecc8054047b6b8630af1a0b36f |
| Source note | uspto-grants-2013_01 |