HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025617Generated: November 1, 2026
Pyridine → 7-(3-(6-tert-butyl-8-fluoro-1-oxophthalazin-2(1H)-yl)-2-(hydroxymethyl)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile
https://huagongshe.com/reaction/1025617
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | 7H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile | HCID 22605269 | — |
| Reactant | 6-tert-butyl-8-fluoro-2-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-4-yl)phthalazin-1(2H)-one | HCID 71008199 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Product | 7-(3-(6-tert-butyl-8-fluoro-1-oxophthalazin-2(1H)-yl)-2-(hydroxymethyl)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile | HCID 71008407 | 31.6% |
Reaction Steps
In a 25 mL round-bottomed flask, 7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile (40.9 mg, 284 μmol, Eq: 1.00), 6-tert-butyl-8-fluoro-2-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-4-yl)phthalazin-1(2H)-one (100 mg, 284 μmol, Eq: 1.00), copper acetate (34.8 mg) and pyridine (44.9 mg, 45.9 μl, 568 μmol, Eq: 2) were combined with dichloroethane to give a dark blue suspension. The reaction mixture was flushed with nitrogen. The reaction mixture was heated to 80° C. and stirred for 16 hr. The reaction was diluted with sat NH4Cl (50 mL) and extracted with EtOAc (3×50 mL). The mixture was separated by flash column using 30-50% EtOAc in hexanes to give the 7-[3-(6-tert-Butyl-8-fluoro-1-oxo-1H-phthalazin-2-yl)-2-hydroxymethyl-phenyl]-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile (42 mg, 31%) as a lyophilized white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729078B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-cd960f89a2bf43c2b84893f4ef84114d |
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| Source note | uspto-grants-2014_05 |
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