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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604872Generated: October 25, 2026

Phosgene → [5-(4-tert-Butyl-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine

https://huagongshe.com/reaction/604872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantMethyl vinyl ketoneHCID 6570—
Reactant4-Tert-ButylanilineHCID 69861—
Reactant[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thioureaHCID 71650841—
Product[5-(4-tert-Butyl-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amineHCID 25106119—

Reaction Steps

The title compound was prepared in analogy to example 7 without purification of the intermediate from 149 mg (1 mmol) 4-tert-butylaniline and 421 mg (6 mmol) methyl vinylketone. The crude chloroketone was used without further purification in the next step with 53 mg (0.2 mmol) [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea. The crude product was purified on silica gel with methylene chloride/methanol 19/1 yielding 45 mg (50%) of [5-(4-tert-butyl-benzyl)-4-methyl-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine as a brown solid. MS ISP (m/e): 447.3 (100) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.12 (s, 1H), 7.63 (s, 1H), 7.53 (s, 1H), 7.32 (d, 2H), 7.22 (s, 2H), 7.15 (d, 2H), 7.01 (s, 1H), 3.92 (s, 2H), 3.77 (s, 3H), 2.24 (s, 3H), 2.13 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910740B2
Source datasetuspto-grants-2011_03
ORD IDord-650227d151cf424eb9a1698219a73e72
Source noteuspto-grants-2011_03