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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366547Generated: October 31, 2026

Diisopropylethylamine → Racemic tris(1,1-dimethylethyl) 2-{2-chloro-6-[1-(dimethylamino)-3-azabicyclo[3.1.0]hex-3-yl]-5-fluoro-4-pyrimidinyl}-1,1,2-hydrazinetricarboxylate

https://huagongshe.com/reaction/1366547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTris(1,1-dimethylethyl) 2-(2,6-dichloro-5-fluoro-4-pyrimidinyl)-1,1,2-hydrazinetricarboxylateHCID 58000755—
Reactantn,n-Dimethyl-3-azabicyclo[3.1.0]hexan-1-amine dihydrochlorideHCID 66936286—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductRacemic tris(1,1-dimethylethyl) 2-{2-chloro-6-[1-(dimethylamino)-3-azabicyclo[3.1.0]hex-3-yl]-5-fluoro-4-pyrimidinyl}-1,1,2-hydrazinetricarboxylateHCID 8721035184.5%

Reaction Steps

To a solution of racemic N,N-dimethyl-3-azabicyclo[3.1.0]hexan-1-amine dihydrochloride (assumed 0.5339 g, 2.681 mmol) in DMF (13 mL) was added tris(1,1-dimethylethyl) 2-(2,6-dichloro-5-fluoro-4-pyrimidinyl)-1,1,2-hydrazinetricarboxylate (1.33 g, 2.674 mmol) and N,N-diisopropylethylamine (1.87 mL, 10.74 mmol). The solution was stirred overnight and then diluted with Et2O (100 mL). The mixture was washed with water (2×50 mL), and the combined aqueous phase was extracted with a fresh portion of Et2O (50 mL). The combined organic phase was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by gradient silica gel chromatography (0% to 100% EtOAc in hexanes; 1% Et3N) to afford racemic tris(1,1-dimethylethyl)2-{2-chloro-6-[1-(dimethylamino)-3-azabicyclo[3.1.0]hex-3-yl]-5-fluoro-4-pyrimidinyl}-1,1,2-hydrazinetricarboxylate (1.3261 g, 84%) as a white foam. LCMS: (M+H)+: 587.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-8e21a69a16954c45bbbc9eb61d520e5f
Source noteuspto-grants-2011_02