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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295665Generated: October 31, 2026

Sodium Sulfate → 6-[4-(4-Ethyl-piperazin-1-ylmethyl)-phenyl]-4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1295665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantAmmonium ChlorideHCID 25517—
Reactant(4-Ethyl-piperazin-1-yl]-[4-[4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-phenyl]-methanoneHCID 10207082—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product6-[4-(4-Ethyl-piperazin-1-ylmethyl)-phenyl]-4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-7H-pyrrolo[2,3-d]pyrimidineHCID 10206303—

Reaction Steps

1.56 ml of diisobutyl-aluminium hydride (1 M in THF) are added to a solution of 130 mg (0.26 mMol) of (4-ethyl-piperazin-1-yl)-{4-[4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-phenyl}-methanone in 13 ml of THF at −15° C. under a N2-atmosphere. After 3 h, 4 ml of EtOAc are added to the solution, followed by 0.2 ml of a saturated solution of NH4Cl in water. After adding solid Na2SO4, the reaction mixture is filtered through Celite. The filtrate is concentrated together with 3 g of SiO2. The resulting powder is put on top of a chromatography column (SiO2) and then eluted with EtOAc/methanol 4:1 and finally EtOAc/methanol/NEt3 80:20:1, yielding the title compound; HPLC (conditions see Examples 67-78) tR=10.5 min; MS-ES+: (M+H)+=485.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244729B2
Source datasetuspto-grants-2007_07
ORD IDord-e61e5a76ce5f432ab2474a6e4504bed6
Source noteuspto-grants-2007_07