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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172316Generated: October 25, 2026

5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride → 5-(2-(1H-Imidazol-1-yl)-4-(trifluoromethyl)phenyl)-N-(5-fluorothiazol-2-yl)-3,4-dihydroisoquinoline-2(1H)-sulfonamide

https://huagongshe.com/reaction/2172316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45074003—
Reactant8-(2-(1H-imidazol-1-yl)-4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolineHCID 89815122—
Reactant5-bromo-N-(5-fluorothiazol-2-yl)-3,4-dihydroisoquinoline-2(1H)-sulfonamideHCID 89815577—
Product5-(2-(1H-Imidazol-1-yl)-4-(trifluoromethyl)phenyl)-N-(5-fluorothiazol-2-yl)-3,4-dihydroisoquinoline-2(1H)-sulfonamideHCID 71736738—

Reaction Steps

The title compound was prepared in a procedure analogous to Intermediate I, wherein 8-(2-(1H-imidazol-1-yl)-4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline (Intermediate R) was substituted for 5-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride [M+H]+=524.0 1H NMR (400 MHZ, Acetone-d6) δ ppm: 7.97 (s, 1H), 7.91 (dd, J=7.9, 1.0 Hz, 1H), 7.70 (d, J=8.0 Hz, 1H), 7.48 (d, J=1.0 Hz, 1H), 7.44 (t, J=1.3 Hz, 1H), 7.10-7.19 (m, 2H), 6.97-7.02 (m, 3H), 4.28-4.41 (m, 2H), 3.68-3.77 (m, 1H), 3.21-3.32 (m, 1H), 2.44-2.54 (m, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051311B2
Source datasetuspto-grants-2015_06
ORD IDord-085b2786236d410680b937bea9f7b26d
Source noteuspto-grants-2015_06