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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452326Generated: October 31, 2026

HCID 58362709, compound → HCID 67300926, compound

https://huagongshe.com/reaction/452326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58362709HCID 58362709—
ReactantHCID 59214162HCID 59214162—
ProductHCID 67300926HCID 6730092635.3%

Reaction Steps

T534 was prepared using general procedure B from 2-bromo-1-(2-fluoroethyl)-1H-benzo[d]imidazole and tert-butyl methyl-4-(ethynyl)phenylcarbamate. Reaction was performed on a 53 mgs scale of 2-bromo-1-(2-fluoroethyl)-1H-benzo[d]imidazole. The crude product was purified by ISCO column to afford tert-butyl 4-((1-(2-fluoroethyl)-1H-benzo[d]imidazol-2-yl)ethynyl)phenyl(methyl)carbamate (0.03 g, 35.3%). It was dissolved in acetonitrile (0.5 mL). To this solution was added a solution of 20% sulfuric acid (1.5 mL, 5.63 mmol). The resulting mixture was stirred at room temperature for 20 minutes, diluted with water (2.0 mL) and purified by preparative HPLC to afford T534 as TFA salt (0.004 g, 12.88%). 1H NMR (400 MHz, CD3CN) δ 7.81-7.79 (m, 1H), 7.67-7.65 (m, 1H), 7.52-7.48 (m, 4H), 6.66-6.64 (m, 2H), 4.95-4.93 (m, 1H), 4.83-4.478 (m, 2H), 4.74-4.73 (m, 1H), 2.82 (s, 3H); MS (ESI): 294.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08491869B2
Source datasetuspto-grants-2013_07
ORD IDord-e5de64fec2bc4edfbd6f3ffba98e58f0
Source noteuspto-grants-2013_07