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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247797Generated: November 2, 2026

N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → 7-[2-(Tert-butoxycarbonylamino)acetyl]amino-2,3-dihydro-1h-imidazo[1,2-b]pyrazole

https://huagongshe.com/reaction/1247797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-amine sulfateHCID 135800725—
SolventDichloromethaneHCID 6344—
Product7-[2-(Tert-butoxycarbonylamino)acetyl]amino-2,3-dihydro-1h-imidazo[1,2-b]pyrazoleHCID 13580073059.5%

Reaction Steps

To a solution of 7-amino-2,3-dihydro-1H-imidazo[1,2-b]pyrazole sulfuric acid salt (1.42 g) and N-ethyldiisopropylamine (2.73 g) in methylene chloride (50 ml) was added N-[2-(tert-butoxycarbonylamino)acetoxy]succinimide (1.90 g). The mixture was stirred at room temperature for 22 hours. The reaction mixture was washed with saturated aqueous sodium hydrogen carbonate solution, and the organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The oily residue was purified by column chromatography on silica gel eluting with 5% methanol/chloroform to give 7-[2-(tert-butoxycarbonylamino)acetyl]amino-2,3-dihydro-1H-imidazo[1,2-b]pyrazole (1.07 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129232B2
Source datasetuspto-grants-2006_10
ORD IDord-40184e3c41ff4f22818621079f21b59d
Source noteuspto-grants-2006_10