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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246208Generated: October 30, 2026

1-Phenoxy-2-propanamine → 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-methyl-2-phenoxy-ethyl)-amide

https://huagongshe.com/reaction/246208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenoxy-2-propanamineHCID 37087—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acidHCID 71279620—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-methyl-2-phenoxy-ethyl)-amideHCID 7128599489%

Reaction Conditions

Temperature25 °C

Reaction Steps

In a 100 mL round-bottomed flask, HBTU (78 mg, 0.21 mmol), Hunig's base (0.14 ml, 0.79 mmol) and 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (70 mg, 0.16 mmol) were combined with DMF (3 ml) to give a light yellow solution. 1-Phenoxypropan-2-amine (48 mg, 0.32 mmol) was added and the reaction mixture was stirred at 25° C. for 16 h. The reaction mixture was diluted with EtOAc. The reaction mixture was poured into 50 mL sat NaHCO3 and extracted with EtOAc (2×50 mL). The organic layers were combined and washed with water (2×50 mL) then dried over MgSO4 and concentrated in vacuo to provide 81 mg (89%) of 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-methyl-2-phenoxy-ethyl)-amide as a white solid. MS: (M+H)+=575.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-5151fb9abab6470e9e32201630f6ca80
Source noteuspto-grants-2014_02