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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182228Generated: October 31, 2026

Sodium hydride → HCID 67158717, compound

https://huagongshe.com/reaction/2182228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 1-bromocyclobutanecarboxylateHCID 97595—
ReactantHCID 22477340HCID 22477340—
SolventDimethylformamideHCID 6228—
ProductHCID 67158717HCID 67158717—

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium hydride (43 mg, 60% dispersion in mineral oil) was added to a stirred solution of 2-(5-hydroxy-6-methoxy-1-methyl-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine [400 mg, Reference Example 28(a)] in dry dimethylformamide (20 mL) under a nitrogen atmosphere at ambient temperature. The mixture was allowed to stir for 1 hour then treated with ethyl-1-bromocyclobutanecarboxylate (216 μl) and stirring was continued overnight. Additional portions of sodium hydride (43 mg, 60% dispersion in mineral oil) and ethyl 1-bromocyclobutanecarboxylate (216 μl) were then added, then the mixture was heated at 50° C. for 5 hours. The cooled reaction mixture was evaporated and the residue was partitioned between ethyl acetate and water. The organic phase was washed with water, then with brine, then dried over magnesium sulfate and then evaporated. The yellow residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and pentane (2:3, v/v) to give the title compound (266 mg) as a yellow oil. MS: 576(MH+). HPLC (METHOD A): RT=11.07 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897207B2
Source datasetuspto-grants-2005_05
ORD IDord-d9262bcbbf754b5bbe11b0f1e4e5a312
Source noteuspto-grants-2005_05