HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452326Generated: October 31, 2026
HCID 58362709, compound → HCID 67300926, compound
https://huagongshe.com/reaction/452326
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 58362709 | HCID 58362709 | — |
| Reactant | HCID 59214162 | HCID 59214162 | — |
| Product | HCID 67300926 | HCID 67300926 | 35.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08491869B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-e5de64fec2bc4edfbd6f3ffba98e58f0 |
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| Source note | uspto-grants-2013_07 |
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