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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437319Generated: November 3, 2026

Tetrahydrofuran → 3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde

https://huagongshe.com/reaction/1437319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant6-(Hydroxymethyl)-2H-pyrido[3,2-b][1,4]thiazin-3(4H)-oneHCID 11608093—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehydeHCID 1159359155.1%

Reaction Steps

A solution of the alcohol (i) (330 mg) in dichloromethane (30 ml)/THF (30 ml) was treated with manganese dioxide (730 mg) and stirred at room temperature. Further manganese dioxide was added after 1 hour (730 mg) and 16 hours (300 mg). After a total of 20 hours the mixture was filtered through kieselguhr and the filtrate evaporated. The product was triturated with EtOAc/hexane (1:1) and collected to give a solid (180 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622481B2
Source datasetuspto-grants-2009_11
ORD IDord-79d88a0e92dc4fdbadf2ba3688f88941
Source noteuspto-grants-2009_11