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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595437Generated: October 25, 2026

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

https://huagongshe.com/reaction/595437

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 numberUS09242975B2
Source datasetuspto-grants-2016_01
ORD IDord-96f990b7d46e4aa9aea3ec384b5a5167
Source noteuspto-grants-2016_01