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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090093Generated: November 1, 2026

Methyl-2-{[4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoate → 2-{[4-(5-Cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoic acid

https://huagongshe.com/reaction/2090093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl-2-{[4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoateHCID 25151228—
Reactant4-(5-Cyano-7-isopropylbenzo[d]oxazol-2-yl)benzoic acidHCID 57369945—
Product2-{[4-(5-Cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoic acidHCID 25152785—

Reaction Steps

The title compound was prepared from methyl-2-{[4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoate (EXAMPLE 29) using procedure analogous to that described in INTERMEDIATE 2, Step C. Mass spectrum (ESI) 406.20 (M+1). 1H NMR (500 MHz, CDCl3): δ 8.19 (d, J=8.4 Hz, 2H), 7.89 (d, J=8.4 Hz, 2H), 7.79 (d, J=1.4 Hz, 1H), 7.38 (s, 1H), 7.02 (d, J=8.4 Hz, 2H), 4.59 (m, 1H), 3.45 (m, 1H), 2.2 m, 1H), 1.32 (d, J=7.10 Hz, 6H), 0.91 (t, J=6.3 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436028B2
Source datasetuspto-grants-2013_05
ORD IDord-a9ce1d6c0ff04e2389eca36dd3a3f827
Source noteuspto-grants-2013_05