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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503352Generated: October 31, 2026

Sodium Hydroxide → HCID 118022968, compound

https://huagongshe.com/reaction/1503352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-2-(methylsulfonyl)pyrimidineHCID 11148232—
ReactantHCID 118023783HCID 118023783—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118022968HCID 11802296889.6%

Reaction Steps

To a solution of N-(3-isobutyryl-1-methyl-1H-indol-5-yl)formamide (450 mg, 1.84 mmol) in anhydrous THF (3 mL) and anhydrous DMF (3 mL) was added 60% NaH (228 mg, 5.52 mmol) at 0° C. After being stirred for 30 min at room temperature, it was cooled to 0° C. To this, was added 4-chloro-2-(methylsulfonyl)pyrimidine (466 mg, 2.43 mmol) and then stirred for 2 hours. Quenching the reaction by addition of ice and 2N solution of sodium hydroxide (2 mL) resulted precipitation of brown solids. Additional 20 mL of water was added to complete of solid formation. The resulted solids were collected by filtration, rinsed with water and the dried in vacuo to provide the desired intermediate 5 as a brown solid (542 mg, 89%); MS (ESI) m/z 329 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212178B2
Source datasetuspto-grants-2015_12
ORD IDord-858668919c5e47e1984e41dc72999d34
Source noteuspto-grants-2015_12