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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401095Generated: November 1, 2026

Diisopropylethylamine → HCID 86711440, compound

https://huagongshe.com/reaction/1401095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 86711429HCID 86711429—
ReactantHCID 86711441HCID 86711441—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86711440HCID 86711440—

Reaction Steps

To solution containing 3-(1-(tert-butoxycarbonyl)-6-fluoro-1H-indol-3-yl)acrylic acid (200.0 mg, 0.66 mmol), 3-fluoro-N′-isopropylbenzohydrazide (192.8 mg, 0.98 mmol) and HATU (376.6 mg, 0.98 mmol) dissolved in DMF (5.0 ml), N,N-diisopropylethylamine (DIPEA)(0.16 ml, 0.98 mmol) was slowly drop-wise added and stirred at room temperature for 12 hr. The reaction mixture was diluted with EtOAc, washed with water and brine, dried with anhydrous MgSO4, filtered, and concentrated under reduced pressure. The residue was separated through silica gel chromatography (50% EtOAc) for refinment and dried so that white (E)-tert-butyl 6-fluoro-3-(3-(2-(3-fluorobenzoyl)-1-isopropylhydrazinyl)-3-oxoprop-1-enyl)-1H-indole-1-carboxylate was obtained (180.0 mg, 56.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906952B2
Source datasetuspto-grants-2014_12
ORD IDord-2799ed15d0f14b3d902990a4e0d63f89
Source noteuspto-grants-2014_12