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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046545Generated: October 31, 2026

1-(2,2,2-Trifluoroacetamido)cyclopropane-1-carboxylic acid → 1-(2,2,2-Trifluoro-acetylamino)-cyclopropanecarboxylic acid ((rac)-5-bromo-7-fluoro-indan-1-yl)-amide

https://huagongshe.com/reaction/2046545

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,2,2-Trifluoroacetamido)cyclopropane-1-carboxylic acidHCID 12988800—
Reactant5-Bromo-7-fluoro-2,3-dihydro-1H-inden-1-amineHCID 68296745—
Product1-(2,2,2-Trifluoro-acetylamino)-cyclopropanecarboxylic acid ((rac)-5-bromo-7-fluoro-indan-1-yl)-amideHCID 123231018—

Reaction Steps

In analogy to the procedure described for the preparation of intermediate A-1 [B] and A-1 [C], (rac)-5-bromo-7-fluoro-indan-1-ylamine has been coupled with 1-(2,2,2-trifluoroacetamido)cyclopropanecarboxylic acid (intermediate A-1 [A]) to give 1-(2,2,2-trifluoro-acetylamino)-cyclopropanecarboxylic acid ((rac)-5-bromo-7-fluoro-indan-1-yl)-amide, which was subsequently reacted with 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) to yield the title compound as light yellow amorphous solid. MS: 455.2 (M−H−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592426B2
Source datasetuspto-grants-2013_11
ORD IDord-51c0fbd57b0c45a29283196fa9818bb2
Source noteuspto-grants-2013_11