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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645685Generated: October 30, 2026

Triethylamine → HCID 25195903, compound

https://huagongshe.com/reaction/645685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 25195690HCID 25195690—
SolventDichloromethaneHCID 6344—
ProductHCID 25195903HCID 2519590318.9%

Reaction Steps

To a suspension of N4-(1H-indazol-6-yl)-N2-(4-(piperazin-1-yl)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine (9 mg, 0.021 mmol) and triethylamine (TEA) (0.010 mL, 0.072 mmol) in CH2Cl2 (1 mL) at room temperature, methanesulfonyl chloride (MeSO2Cl) (0.006 mL, 0.077 mmol) was added. After being stirred at room temperature for 3 h, the mixture was concentrated in vacuo. The residue was purified by HPLC to give N4-(1H-indazol-6-yl)-N2-(4-(4-(methylsulfonyl)piperazin-1-yl)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine (2 mg), MS 504.3 (M+H) (Compound 8-1); and N4-(1-(methylsulfonyl)-1H-indazol-6-yl)-N2-(4-(4-(methylsulfonyl)piperazin-1-yl)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine (1 mg), MS 582.4 (M+H) (Compound 8-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705004B2
Source datasetuspto-grants-2010_04
ORD IDord-7942d3997fdf484da4826c0522d40707
Source noteuspto-grants-2010_04