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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295051Generated: November 1, 2026

2-(2-{[(Tert-butoxy)carbonyl]amino}acetamido)acetic acid → 4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenyl N-(tert-butoxycarbonyl)glycylglycinate

https://huagongshe.com/reaction/1295051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-{[(Tert-butoxy)carbonyl]amino}acetamido)acetic acidHCID 333466—
Reactant4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenolHCID 135524867—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenyl N-(tert-butoxycarbonyl)glycylglycinateHCID 68884164—

Reaction Steps

A solution of 4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenol (0.30 g, 1.0 mmol), N-(tert-butoxycarbonyl)glycylglycine (0.232 g, 1.0 mmol), N,N-dicylohexylcarbodiimide (0.206 g, 1.0 mmol) and DMAP (0.122 g, 1.0 mmol) in 10 mL of CH2Cl2 was stirred overnight at ambient temperature. The reaction mixture was diluted with CH2Cl2 and filtered through a plug of silica gel. The gel was rinsed with additional CH2Cl2. The combined filtrates were concentrated in vacuo to give 0.35 g to the title compound as a white solid, mp 103–104° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241791B2
Source datasetuspto-grants-2007_07
ORD IDord-532644139a504b3289f3d36f359c17ee
Source noteuspto-grants-2007_07