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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472897Generated: October 29, 2026

1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine → HCID 67215697, compound

https://huagongshe.com/reaction/472897

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
ReactantImidazo[1,5-a]pyridine-6-carboxylic acidHCID 22565897—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 67215697HCID 67215697—

Reaction Conditions

Temperature90 °C

Reaction Steps

3.37 ml (14.06 mmol) of N,N-dimethylformamide di(tert-butyl)acetal are added to 570 mg (3.52 mmol) of imidazo[1,5-a]pyridine-6-carboxylic acid [described in Bioorg. Med. Chem. Lett., (2002), 12(3), 465-470] in a mixture of 5 ml of dimethylformamide and 5 ml of toluene and the mixture is heated at 90° C. for 6 hours. 3.37 ml (14.06 mmol) of N,N-dimethylformamide di(tert-butyl)acetal are again added to the reaction medium and the mixture is heated at 90° C. for a further 4 hours. The reaction medium is poured onto water and extracted with ethyl acetate. The organic phase is separated by settling, washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. The product is purified by filtration through a bed of silica, elution being carried out with a mixture of dichloromethane and methanol (98/2). After evaporation, 580 mg of a beige powder are obtained. Melting point: 77° C.; 1H NMR (d6-DMSO): 1.59 (9H, s), 7.71 (1H, d), 7.36 (1H, s), 7.58 (1H, d), 8.56 (1H, s), 9.03 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633216B2
Source datasetuspto-grants-2014_01
ORD IDord-09cea92ea4294e91832c3a74c97d3153
Source noteuspto-grants-2014_01