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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431861Generated: November 4, 2026

(alphaR)-alpha-((Methoxycarbonyl)amino)benzeneacetic acid → HCID 178495707, compound

https://huagongshe.com/reaction/1431861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(alphaR)-alpha-((Methoxycarbonyl)amino)benzeneacetic acidHCID 10910775—
Reactant(1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphateHCID 75951468—
ReactantHCID 178495693HCID 178495693—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 178495707HCID 178495707—

Reaction Steps

A mixture of (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (22 mg, 0.105 mmol), COMU (45 mg, 0.069 mmol), and tert-butyl (2S,4S)-4-(methoxymethyl)-2-(5-{2-[(25)-pyrrolidin-2-yl]-1,11-dihydroisochromeno[4′,3′:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (65 mg, 0.105 mmol) in 1.5 mL 10% DIPEA in DMF was stirred for 1.5 h. The reaction mixture was partitioned between ethyl acetate and saturated sodium bicarbonate. The organic phase was dried over sodium sulphate, filtered and concentrated under reduced pressure. The crude intermediate was treated with 8 mL 1.25N HCl in ethanol at 50° C. for 4 h. Added saturated sodium bicarbonate and extracted the free base into dichloromethane. (106 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940718B2
Source datasetuspto-grants-2015_01
ORD IDord-004f9900fd504f61bc575471db251193
Source noteuspto-grants-2015_01