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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890430Generated: October 31, 2026

6-amino-3,4-dihydro-2H-1,4-benzothiazin-3-one → HCID 67222622, compound

https://huagongshe.com/reaction/1890430

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-amino-3,4-dihydro-2H-1,4-benzothiazin-3-oneHCID 686901—
ReactantHCID 11217932HCID 11217932—
SolventWater ethanolHCID 19096565—
ProductHCID 67222622HCID 6722262283%

Reaction Steps

A solution of 6-amino-4H-benzo[1,4]thiazin-3-one (10.68 g, 59.3 mmol; commercial) and (2R)-tert-butyl-dimethyl-(2-oxiranyl-ethoxy)-silane (first eluting compound of step C.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 Et2O/MeOH followed by filtration. The filtrate 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507478B2
Source datasetuspto-grants-2013_08
ORD IDord-e34d665846a94cccb22ddbe084862f60
Source noteuspto-grants-2013_08