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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714102Generated: October 29, 2026

(rac)-Cyclopropanesulfonic acid [4-(3-fluoro-4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-yl]-amide → (rac)-Cyclopropanesulfonic acid [4-(4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-yl]-amide

https://huagongshe.com/reaction/714102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(rac)-Cyclopropanesulfonic acid [4-(3-fluoro-4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-yl]-amideHCID 71811527—
Reactant(rac)-4-(4-Trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-ylamineHCID 89846378—
Product(rac)-Cyclopropanesulfonic acid [4-(4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-yl]-amideHCID 718114944%

Reaction Steps

In analogy to the procedure described for the preparation of (rac)-cyclopropanesulfonic acid [4-(3-fluoro-4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-yl]-amide (example 91), replacing (rac)-4-(3-fluoro-4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-ylamine with (rac)-4-(4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindin-7-ylamine (example 93). The title compound was obtained as a light brown oil in 4% yield. MS: 383.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187429B2
Source datasetuspto-grants-2015_11
ORD IDord-a0a9fb8dc60c403185435d7cf7c90c17
Source noteuspto-grants-2015_11