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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248818Generated: October 26, 2026

Sodium Carbonate → N,N-dimethyl-alpha,alpha-diphenyl-4-[[9-(2-pyridinylmethyl)-9H-purin-8-yl]amino]-1-piperidinebutanamide

https://huagongshe.com/reaction/2248818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDimethylacetamideHCID 31374—
Reactant(Dihydro-3,3-diphenyl-3H-furan-2-ylidene)dimethylammonium bromideHCID 2723589—
ReactantN-(4-piperidinyl)-9-(2-pyridinylmethyl)-9H-purin-8-amineHCID 19785321—
SolventWaterHCID 962—
ProductN,N-dimethyl-alpha,alpha-diphenyl-4-[[9-(2-pyridinylmethyl)-9H-purin-8-yl]amino]-1-piperidinebutanamideHCID 5378290971%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3.46 parts of N-(dihydro-3,3-diphenyl-2(3H)-furanylidene)-N-methylmethanaminium bromide, 3.1 parts of N-(4-piperidinyl)-9-(2-pyridinylmethyl)-9H-purin-8-amine, 1.5 parts of sodium carbonate and 45 parts of N,N-dimethylacetamide was stirred overnight at 80° C. after cooling, the reaction mixture was poured into water and 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 eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 4.1 parts (71%) of N,N-dimethyl-α,α-diphenyl-4-[[9-(2-pyridinylmethyl)-9H-purin-8-yl]amino]-1-piperidinebutanamide; mp. 191.6° C. (compound 122).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041448
Source datasetuspto-grants-1991_08
ORD IDord-f439600a495c401ca922974c90688a20
Source noteuspto-grants-1991_08