Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808387Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 59483777, compound

https://huagongshe.com/reaction/1808387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-(Pyridin-4-yl)-3,9-diazaspiro[5.5]undecaneHCID 15940811—
Reactant7-(tert-Butoxycarbonyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylic acidHCID 44558548—
SolventDichloromethaneHCID 6344—
ProductHCID 59483777HCID 5948377763%

Reaction Steps

DIPEA (5.96 mmol, 4.0 equiv.), EDCl (2.24 mmol, 1.5 equiv.) and HOBt (2.24 mmol, 1.5 equiv.) were added at 0° C. to a solution of 7-(tert-butoxycarbonyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylic acid (1.49 mmol, 1.0 equiv.) in DCM (20 ml), and the mixture was stirred for 30 min. A solution of 3-(pyridin-4-yl)-3,9-diazaspiro[5.5]undecane (F-19) (1.49 mmol, 1.0 equiv.) in DCM (5 ml) was added at 0° C., and then the reaction mixture was stirred for 16 h at 25° C. The mixture was diluted with DCM (100 ml) and washed with sat. sodium carbonate solution (65 ml), sat. ammonium chloride solution (65 ml), water (50 ml) and sat. sodium chloride solution (50 ml), dried over Na2SO4 and concentrated in vacuo. The resulting crude product was used directly in the following stage. Yield: 63%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357717B2
Source datasetuspto-grants-2013_01
ORD IDord-c147575b3e3941c5b61aa1258834be3e
Source noteuspto-grants-2013_01