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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309636Generated: November 2, 2026

Water → HCID 86741816, compound

https://huagongshe.com/reaction/2309636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 14013372HCID 14013372—
Reactant7-(2-bromoethyl)-3,4-dihydro-8-methyl-2H,6H-pyrimido[2,1-b][1,3]thiazin-6-one monohydrobromideHCID 15586466—
SolventDimethylformamideHCID 6228—
ProductHCID 86741816HCID 8674181661%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3.14 parts of 7-(2-bromoethyl)-3,4-dihydro-8-methyl-2H,6H-pyrimido[2,1-b][1,3]thiazin-6-one monohydrobromide, 3.5 parts of 3-[(4-fluorophenyl)methyl]-2-(4-piperidinylmethyl)-3H-imidazo[4,5-b]pyridin, 4 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylformamide was stirred and heated overnight at 70° C. After cooling, water was added. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluant. The pure fractions were collected and the eluent was evaporated. The residue was converted into the ethanedioate salt in ethanol. The salt was filtered off and dried, yielding 3.7 parts (61%) of 7-[2-[4-[[3 -[(4-fluorophenyl)methyl]-3H-imidazo[4,5-b]pyridin-2-yl]methyl]-1-piperidinyl]ethyl]-3,4-dihydro-8-methyl-2H,6H-pyrimido[2,1-b][1,3]thiazin-6-one ethanedioate (1:2); mp. 190.5° C. (205).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695575
Source datasetuspto-grants-1987_09
ORD IDord-3988e34d4f574023b7af2a6ae9a961d4
Source noteuspto-grants-1987_09