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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886408Generated: October 31, 2026

Water → HCID 86745285, compound

https://huagongshe.com/reaction/1886408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant3-(2-Chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one--hydrogen chloride (1/1)HCID 15605782—
ReactantHCID 19875944HCID 19875944—
SolventDimethylacetamideHCID 31374—
ProductHCID 86745285HCID 8674528551.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4.2 parts of 3-(2-chloroethyl)-6,7,8,9-tetrahydro-2-methyl-4H-pyrido [1,2-a]pyrimidin-4-one monohydrochloride, 6.9 parts of N-(3-pyrrolidinyl)-1-(4-thiazolylmethyl)-1H-benzimidazol-2-amine dihydrobromide, 9.7 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylacetamide was stirred for 1.5 hour at 100° C. After cooling, the reaction mixture was poured into 500 parts of water. The product was extracted three times with dichloromethane. The combined extracts were washed with water, dried, filtered and evaporated. The oily residue was converted into the (E)-2-butenedioate salt in 180 parts of 2-propanone and ethanol. The salt was filtered off and dried, yielding 6 parts (51.2%) of 6,7,8,9-tetrahydro-2-methyl-3-[2-[3-[[1-(4-thiazolylmethyl)-1H-benzimidazol-2-yl]amino]-1-pyrrolidinyl]-ethyl]-4H-pyrido[1,2-a]pyrimidin-4-one (E)-2-butenedioate(2:5); mp. 148.1° C. (compound 59).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151424
Source datasetuspto-grants-1992_09
ORD IDord-8e670b36b1024b80b3deb65c539027ca
Source noteuspto-grants-1992_09