HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521529Generated: October 30, 2026
2,4-Dichloro-5-(trifluoromethyl)pyrimidine → HCID 89815972, compound
https://huagongshe.com/reaction/1521529
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichloro-5-(trifluoromethyl)pyrimidine | HCID 2782774 | — |
| Reactant | (R)-methyl 1-isopropyl-7-(methylsulfonyl)-1,2,3,4-tetrahydrobenzo[4,5]imidazo[1,2-a]pyrazine-8-carboxylate | HCID 89815671 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 89815972 | HCID 89815972 | 42.6% |
Reaction Steps
To a solution of 2,4-dichloro-5-(trifluoromethyl)pyrimidine (20.0 mg, 0.092 mmol) in DCE (1 mL) and t-BuOH (1 mL) was added ZnCl2 (1M in diethyl ether, 0.2 mL, 0.2 mmol) at 0° C. The mixture was stirred at 0° C. for 1 h. Then a solution of (R)-methyl 1-isopropyl-7-(methylsulfonyl)-1,2,3,4-tetrahydrobenzo[4,5]imidazo[1,2-a]pyrazine-8-carboxylate (31 mg, 0.09 mmol) in DCE (1 mL) and t-BuOH (1 mL) was added to the reaction mixture via syringe over 1 min at 0° C. After addition, the resulting mixture was stirred at rt overnight. The reaction mixture was concentrated under vacuum. Water (5 mL) and EtOAc (5 mL) were added to the mixture. The aqueous phase was extracted with EtOAc (3×10 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated under vacuum. The residue was purified by preparative TLC to afford (R)-methyl 2-(4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)-1-isopropyl-7-(methylsulfonyl)-1,2,3,4-tetrahydrobenzo[4,5]imidazo[1,2-a]pyrazine-8-carboxylate (20 mg, 42.6% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073931B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-ba33c0ad842046cd9e6f71c9f009af8b |
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| Source note | uspto-grants-2015_07 |
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