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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398018Generated: November 1, 2026

N-((1,1-dimethylethoxy)carbonyl)-beta-alanine → HCID 58423379, compound

https://huagongshe.com/reaction/1398018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
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 86657371HCID 86657371—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58423379HCID 58423379—

Reaction Conditions

Temperature50 °C

Reaction Steps

A 50 mL vial was charged with a magnetic spin bar, (Z)-5-((2-(piperazin-1-yl)pyridin-3-yl)methylene)thiazolidine-2,4-dione hydrochloride (Example 89) (0.125 g, 0.38 mmol), 3-(tert-butoxycarbonylamino)propanoic acid (0.109 g, 0.57 mmol), DMF (1.912 ml), and diisopropylethylamine (0.334 ml, 1.91 mmol). With stirring, HATU (0.291 g, 0.76 mmol) was added and the reaction was warmed to 50° C. for 3 h. The reaction was then diluted with water and extracted with ethyl acetate (3×50 mL). The combined organic extract was dried with MgSO4, filtered through a bed of Celite, and conc. in vacuo to yield the product which was purified via silica gel chromatography (80 g) using ethyl acetate/hexanes (1:1) as eluent to provide the title compound as an off white solid. (0.080 g, 45.3%); m/z 462.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901307B2
Source datasetuspto-grants-2014_12
ORD IDord-f9bad571fb0a4705a021138741bb7e71
Source noteuspto-grants-2014_12