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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947032Generated: November 2, 2026

Diisopropylethylamine → HCID 59743422, compound

https://huagongshe.com/reaction/1947032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 21882552HCID 21882552—
ReactantHCID 69308463HCID 69308463—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 59743422HCID 59743422—

Reaction Conditions

Temperature130 °C

Reaction Steps

N-(4-amino-cyclohexyl)-N-methyl-methanesulfonamide (567 mg, 2.12 mmol) and DIEA (0.44 mL) were stirred in NMP (0.7 mL) at RT for 1 h. [1-(2-Methanesulfinyl-pyrimidin-4-yl)-1H-indol-4-ylmethyl]-(2-methoxyethyl)-methyl-amine (305 mg, 0.85 mmol) in NMP (0.8 mL) was added, and the tube sealed and heated to 130° C. for 1 h. The mixture was then cooled to RT, decanted into water, stirred at RT overnight, and the filtrate filtered off and dried in vacuo, dissolved in DCM/ether, the precipitate filtered off, and the residue concentrated and crystallized from DCM/ether to yield N-{4-[4-(4-{[(2-methoxy-ethyl)-methyl-amino]-methyl}-indol-1-yl)-pyrimidin-2-ylamino]-cyclohexyl}-N-methyl-methanesulfonamide (Compound 203).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399462B2
Source datasetuspto-grants-2013_03
ORD IDord-2536c5477e344e3c9f5863633c8b02b7
Source noteuspto-grants-2013_03