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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245867Generated: October 25, 2026

Diisopropylethylamine → 2-(3-chloro-6-fluoro-imidazo[1,5-a]pyridin-1-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-2-methoxy-1-methyl-ethyl)-amide

https://huagongshe.com/reaction/245867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(S)-1-methoxypropan-2-amine hydrochlorideHCID 54596079—
Reactant2-(3-chloro-6-fluoro-imidazo[1,5-a]pyridin-1-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acidHCID 71280345—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(3-chloro-6-fluoro-imidazo[1,5-a]pyridin-1-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-2-methoxy-1-methyl-ethyl)-amideHCID 7128816144%

Reaction Steps

A round-bottomed flask was charged with 2-(3-chloro-6-fluoro-imidazo[1,5-a]pyridin-1-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (90 mg, 0.16 mmol) and (S)-1-methoxypropan-2-amine hydrochloride (40 mg, 0.32 mmol). DMF (1 ml) was added followed by N,N-diisopropylethylamine (0.1 ml, 0.57 mmol) and HATU (71 mg, 0.19 mmol). The reaction mixture was stirred at room temperature overnight then water was added. The resulting suspension was filtered, washing with water and petroleum ether. The brown powder was chromatographed over silica gel with MeOH/CH2Cl2/0.5% NH4OH (gradient 0-2% MeOH) to afford 37 mg (44%) of 2-(3-chloro-6-fluoro-imidazo[1,5-a]pyridin-1-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-2-methoxy-1-methyl-ethyl)-amide as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-e386c90466514b459b763b40def97a9b
Source noteuspto-grants-2014_02