HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475856Generated: October 29, 2026
HCID 58075838, compound → HCID 58075657, compound
https://huagongshe.com/reaction/475856
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 58075838 | HCID 58075838 | — |
| Catalyst | HCID 178479819 | HCID 178479819 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 58075657 | HCID 58075657 | 91.5% |
Reaction Steps
To a solution of 1-(2-chloro-6-(methylamino)-5-vinylpyrimidin-4-yl)-1-phenylbut-3-en-1-ol (60 mg) in benzene (5 mL) was added Grubbs I (16 mg), and the reaction mixture was heated at 85° C. for 1 h. The solvent was removed, and the residue was purified by preparative TLC eluting with 40% EtOAc/Hexanes to give the title compound as a colorless oil (50 mg). 1H NMR (500 MHz, CDCl3) δ ppm 7.4 (5H, m), 6.25 (1H, m), 6.07 (1H, m), 5.14 (1H, br. S), 4.52 (1H, s), 3.10 (3H, d<J=5.0 Hz), 2.99 (2H, m). 13C NMR (125 MHz, CDCl3) 164.32, 159.38, 158.85, 144.15, 128.24, 128.02, 127.83, 125.51, 117.54, 108.14, 60.51, 38.50, and 28.57. HRMS calcd. for C15H15ClN3O (M+H) 288.0904. found: 288.0899.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637525B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-50468428f490428d8c67c36c18d16d34 |
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| Source note | uspto-grants-2014_01 |
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