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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046601Generated: November 1, 2026

3-Methylisoxazole-5-carboxylic acid → 3-Methyl-isoxazole-5-carboxylic acid (3-{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-ylcarbamoyl}-oxetan-3-yl)-amide

https://huagongshe.com/reaction/2046601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylisoxazole-5-carboxylic acidHCID 853085—
Reactant3-Amino-oxetane-3-carboxylic acid {(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-yl}-amideHCID 60141040—
Product3-Methyl-isoxazole-5-carboxylic acid (3-{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-ylcarbamoyl}-oxetan-3-yl)-amideHCID 60141181—

Reaction Steps

In analogy to the procedures described for the preparation of intermediate A-1 [B], 3-amino-oxetane-3-carboxylic acid{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-yl}-amide (example 49) was coupled with 3-methyl-isoxazole-5-carboxylic acid to yield the title compound as light yellow oil. MS: 552.1 (MH+, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592426B2
Source datasetuspto-grants-2013_11
ORD IDord-6852b33c1c04497a88d3e3f359b8de47
Source noteuspto-grants-2013_11