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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704732Generated: October 30, 2026

Water → HCID 131716772, compound

https://huagongshe.com/reaction/704732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantDimethylacetamideHCID 31374—
Reactant2-ChloropyrimidineHCID 74404—
ReactantHCID 15037417HCID 15037417—
ProductHCID 131716772HCID 13171677232.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1.7 parts of 2-chloropyrimidine, 4.1 parts of N-[1-(2-aminoethyl)-3-pyrrolidinyl]-3-(4-thiazolylmethyl)-3H-imidazo[4,5-b]-pyridin-2-amine, 2.1 parts of sodium carbonate and 108 parts of N,N-di-methylacetamide was stirred for 6 hours at 100° C. After cooling, the reaction mixture was poured into 600 parts of water and the product was extracted with dichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was converted into the (E)-2-butenedioate salt in 2-propanone and ethanol. The salt was filtered off, washed with 2-propanone and crystallized from a mixture of 2,2'-oxybispropane and methanol (1:1 by volume). The product was filtered off, washed with 2-propanone and dried in vacuo at 60° C., yielding 3.0 parts (32.1%) of N-[1-[2-(2-pyrimidinylamino)ethyl]-3-pyrrolidinyl]-3-(4-thiazolylmethyl)-3H-imidazo[4,5-b]pyridin-2-amine (E)-2-butenedioate(1:3), hemihydrate; mp. 161.7° C. (compound 155).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988689
Source datasetuspto-grants-1991_01
ORD IDord-ccae067b4a744da3b1363cce04d3b252
Source noteuspto-grants-1991_01