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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447728Generated: October 29, 2026

Diisopropylethylamine → HCID 135882282, compound

https://huagongshe.com/reaction/447728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 67104078HCID 67104078—
Reactant2-(3-(1H-imidazol-2-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl)acetic acidHCID 136174646—
SolventDimethylformamideHCID 6228—
ProductHCID 135882282HCID 135882282—

Reaction Conditions

Temperature45 °C

Reaction Steps

A vial was charged with 2-(3-(1H-imidazol-2-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl)acetic acid (55 mg, 0.226 mmol), HBTU (125 mg, 0.33 mmol), 1-(4-Chloro-3-methyl-phenyl)-piperazine dihydrochloride (142 mg, 0.50 mmol), anhydrous DMF (2.0 mL), and DIPEA (0.5 mL). The vial was capped, heated to 45° C., and stirred overnight. The following day, the volatiles were removed in vacuo and separation by preparative hplc (reverse phase, acetonitrile-water gradient) gave 1-[4-(4-Chloro-3-methyl-phenyl)-piperazin-1-yl]-2-[3-(1H-imidazol-2-yl)-pyrazolo[3,4-b]pyridin-1-yl]-ethanone: MS (ES) [M+H]+ found: 436.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481545B2
Source datasetuspto-grants-2013_07
ORD IDord-ba7fe3d1b2674e1dbe36d7725df93a5d
Source noteuspto-grants-2013_07