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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046578Generated: November 1, 2026

2-Methoxypyrimidine-5-carboxylic acid → 2-Methoxy-pyrimidine-5-carboxylic acid (1-{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-ylcarbamoyl}-cyclopropyl)-amide

https://huagongshe.com/reaction/2046578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxypyrimidine-5-carboxylic acidHCID 6486618—
Reactant1-Amino-cyclopropanecarboxylic acid{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-yl}-amideHCID 60142569—
Product2-Methoxy-pyrimidine-5-carboxylic acid (1-{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-ylcarbamoyl}-cyclopropyl)-amideHCID 57523216—

Reaction Steps

In analogy to the procedures described for the preparation of intermediate A-1 [B], 1-amino-cyclopropanecarboxylic acid{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-yl}-amide (example 24) was coupled with 2-methoxy-pyrimidine-5-carboxylic acid to yield the title compound as light yellow solid. MS: 563.2 (MH+, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592426B2
Source datasetuspto-grants-2013_11
ORD IDord-2ec196654c6c4552b1886bace2049d1f
Source noteuspto-grants-2013_11