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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751563Generated: October 28, 2026

(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid → HCID 67682203, compound

https://huagongshe.com/reaction/1751563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acidHCID 10942966—
Reactant(S)-2-(Methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic acidHCID 59264488—
Reactant(S)-benzyl 1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-oxopyrrolidine-2-carboxylateHCID 59610664—
ReactantHCID 86648889HCID 86648889—
ReactantHCID 131733631HCID 131733631—
ProductHCID 67682203HCID 67682203—

Reaction Steps

The title compound was prepared according to the method employed to prepare (S)-benzyl 1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-oxopyrrolidine-2-carboxylate, except that (R)-2-(diethylamino)-2-phenyl-1-((S)-2-(5-(4-(6-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)naphthalen-2-yl)phenyl)-1H-imidazol-2-yl)pyrrolidin-1-yl)ethanone 4HCl salt and (S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic acid were used instead of (S)-benzyl 4-oxopyrrolidine-2-carboxylate hydrochloride and (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid. MS (ESI) m/z 863.81 [M+H]+. (34 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-7d460f0762ac44fd9a5305c52f5e3f85
Source noteuspto-grants-2015_10