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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435877Generated: October 31, 2026

Sodium Sulfate → HCID 10434288, compound

https://huagongshe.com/reaction/1435877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehydeHCID 11593591—
ReactantHCID 68443036HCID 68443036—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 10434288HCID 1043428830.2%

Reaction Steps

To a stirred solution of 2-[6-(6-methoxy[1,5]naphthyridin-4-yl)pyridin-3-yl]ethylamine (0.94 mmole) in dry CH2Cl2 (25 mL) and dry EtOH (10 mL) at RT was added 3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carboxaldehyde (0.18 g, 0.94 mmole) and Na2SO4 (500 mg). After 24 h, the reaction contents were concentrated and dried under high vacuum. To a stirred solution of the crude imine in dry EtOH (25 mL) at RT was added NaBH4 (36 mg, 0.94 mmole). After 24 h, the reaction solution was concentrated under vacuum and to the residue was added 1M HCl (5 mL) and EtOAc (50 mL). After stirring for 1 h, 6M NaOH (1 mL) was added and the organic layer was separated, dried (Na2SO4) and concentrated. Purification on reverse-phase HPLC (CH3CN/H2O, 10-90%) afforded the title compound (0.13 g, 30%) as light yellow solid: 1H NMR (400 MHz, CDCl3) δ 9.89 (br s, 1H), 9.15 (m, 1H), 8.90 (m, 1H), 8.57 (d, J=9.1 Hz, 1H), 8.45 (d, J=9.1 Hz, 1H), 8.20 (m, 2H), 7.51 (m, 1H), 7.22 (d, J=9.1 Hz, 1H), 6.88 (d, J=7.9 Hz, 1H), 4.24 (m, 2H), 4.02 (s, 3H), 3.55 (m, 2H), 3.41 (m, 2H), 3.30 (s, 2H). LC-MS (ES) m/e 459 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618959B2
Source datasetuspto-grants-2009_11
ORD IDord-9b8093dea01b4f8bb102027cc7695c02
Source noteuspto-grants-2009_11