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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877578Generated: October 31, 2026

Diisopropylethylamine → Tert-butyl (1-(2-(6-chloro-4-(isopropylamino)nicotinoyl)hydrazinyl)-3-hydroxy-1-oxopropan-2-yl)carbamate

https://huagongshe.com/reaction/877578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acidHCID 294907—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant6-Chloro-4-(isopropylamino)nicotinohydrazideHCID 89689668—
SolventDimethylformamideHCID 6228—
ProductTert-butyl (1-(2-(6-chloro-4-(isopropylamino)nicotinoyl)hydrazinyl)-3-hydroxy-1-oxopropan-2-yl)carbamateHCID 131732603—

Reaction Steps

To a stirred solution of 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoic acid (500 mg, 2.4 mmol) and 6-chloro-4-(isopropylamino)nicotinohydrazide (10) (2.6 mmol, 1.1 equiv.) in DMF (10 mL), DIPEA (12 mmol, 5 equiv.) and HATU (2.6 mmol, 1.1 equiv.) were added and stirred overnight at room temperature. The reaction mass was concentrated under reduced pressure to remove excess of solvent present. Diluted the residue with EtOAc and washed water followed by brine solution. The organic layer was collected, dried over Na2SO4, filtered and concentrated to get tert-butyl (1-(2-(6-chloro-4-(isopropylamino)nicotinoyl)hydrazinyl)-3-hydroxy-1-oxopropan-2-yl)carbamate (53).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987311B2
Source datasetuspto-grants-2015_03
ORD IDord-076bd0ad0fef4aa69cdd5cb699cbf59a
Source noteuspto-grants-2015_03