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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771849Generated: October 30, 2026

Diisopropylethylamine → HCID 71272465, compound

https://huagongshe.com/reaction/1771849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(3-(aminomethyl)pyridin-2-yl)-N-methylmethanesulfonamideHCID 45480403—
ReactantHCID 71272237HCID 71272237—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 71272465HCID 71272465—

Reaction Conditions

Temperature170 °C

Reaction Steps

4-Chloro-2-(4-fluorophenyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile (30 mg, 0.11 mmol), N-(3-aminomethylpyridin-2-yl)-N-methylmethanesulfonamide (159 mg, 0.552 mmol) and N-ethyldiisopropylamine (0.282 ml, 1.656 mmol) are suspended in 0.4 ml of 1-methyl-2-pyrrolidone and heated in a microwave at 170° C. for 40 min. The reaction is still not complete even after a further 40 min, so that a further equivalent of N-(3-aminomethylpyridin-2-yl)-N-methylmethanesulfonamide (31.8 mg, 0.110 mmol) is added, and the batch is heated at 170° C. for a further 60 min. For work-up, the batch is partitioned between water and ethyl acetate, the organic phase is dried (Na2SO4) and evaporated, giving a brown oil, which is purified by chromatography; yield: 17 mg (34%); LC-MS: 451 [M+H]+; HPLC: 3.07 (RT/min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249140B2
Source datasetuspto-grants-2016_02
ORD IDord-e9fc8ba602f64eb8a8c288835fa9c91b
Source noteuspto-grants-2016_02