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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246609Generated: October 30, 2026

Water → HCID 71280109, compound

https://huagongshe.com/reaction/246609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acidHCID 71279639—
ReactantHCID 86678000HCID 86678000—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 71280109HCID 7128010942.8%

Reaction Steps

To a stirred solution of 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (100 mg, 0.32 mmol) in 6 mL of DMF were added EDCI (123 mg, 0.64 mmol), 4-(tert-butyldimethylsilyloxy)-2-methylbutan-2-amine (139 mg, 0.64 mmol) and DMAP (78 mg, 0.64 mmol) in one portion at room temperature and stirred for 16 hours. The reaction mixture was poured into 35 mL of water filtered and the solid obtained was passed through a pad of silica gel (200-300 mesh, eluting with a mixture of methanol and ethyl acetate (1:20, v/v) to give N-(4-(tert-butyldimethylsilyloxy)-2-methylbutan-2-yl)-2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (70 mg, 42.8%) as a pale yellow solid which was used for the next step without further purification. MS: (M+H)+=511.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-5649c9f97c614592b3bb352f15f10a2e
Source noteuspto-grants-2014_02