HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363134Generated: November 5, 2026
Diisopropylethylamine → 2-(1H-Benzo[d]imidazol-1-yl)-N-((R)-8-fluorochroman-4-yl)-5-nitropyrimidin-4-amine
https://huagongshe.com/reaction/1363134
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dichloro-5-nitropyrimidine | HCID 521266 | — |
| Reactant | (R)-8-fluorochroman-4-amine | HCID 46911919 | — |
| Reactant | (R)-2-chloro-N-(8-fluorochroman-4-yl)-5-nitropyrimidin-4-amine | HCID 59704905 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1H-Benzo[d]imidazol-1-yl)-N-((R)-8-fluorochroman-4-yl)-5-nitropyrimidin-4-amine | HCID 59704935 | — |
Reaction Steps
(R)-8-fluorochroman-4-amine (60 mg, Example 29) was added to a solution of 2,4-dichloro-5-nitropyrimidine (70 mg) and DIEA (0.14 mL) in THF (5 mL) at −78° C. The reaction mixture was stirred for a further 15 min at −78° C. then removed from the cold bath and allowed to warm to RT. A one molar solution of the sodium salt of benzimidazole (0.7 ml, stock solution prepared via the addition of sodium hydride to a benzimidazole solution in THF) was added to the reaction intermediate ((R)-2-chloro-N-(8-fluorochroman-4-yl)-5-nitropyrimidin-4-amine) and the resulting mixture was stirred at RT overnight. Purification via column chromatography (elution with 1 MeOH/DCM) gave the titled compound (120 mg), MH+=407.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884109B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-2e1923ff88af41a9beac9615a5acfd41 |
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| Source note | uspto-grants-2011_02 |
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