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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717421Generated: October 29, 2026

2-(4-(Trifluoromethyl)phenyl)quinazoline-4-carboxylic acid → 2-[[2-(4-(Trifluoromethyl)phenyl)quinazolin-4-yl]carbonyl]-5-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/717421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(Trifluoromethyl)phenyl)quinazoline-4-carboxylic acidHCID 90410579—
Reactant6-Methoxy-1,2,3,4-tetrahydroisoquinolin-5-ol hydrochlorideHCID 90411180—
Product2-[[2-(4-(Trifluoromethyl)phenyl)quinazolin-4-yl]carbonyl]-5-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinolineHCID 8626881415%

Reaction Steps

Reaction of 2-(4-(trifluoromethyl)phenyl)quinazoline-4-carboxylic acid with 5-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride gave compound 37 (15% yield) as off-white oil. 1H NMR (300 MHz, DMSO-d6) δ 2.62 and 2.91 (2t, 2H), 3.50 and 4.04 (2t, 2H), 3.74 and 3.80 (2s, 3H), 4.40 and 4.93 (2s, 2H), 6.31 and 6.77 (2d, 1H), 6.71 and 6.91 (2d, 1H), 7.26-7.84 (m, 1H), 7.90-8.02 (m, 3H), 8.11-8.24 (m, 2H), 8.68-8.76 (m, 3H); MS (ESI) m/z 480 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193707B2
Source datasetuspto-grants-2015_11
ORD IDord-a7082af79a9549538a0c34a86d24dbec
Source noteuspto-grants-2015_11