HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889775Generated: October 31, 2026
Phenyl isocyanate → 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3'-O-phenylcarbamoyl-uridine
https://huagongshe.com/reaction/889775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | HCID 3619573 | HCID 3619573 | — |
| Reactant | 5'-O-(Bis(4-methoxyphenyl)phenylmethyl)uridine | HCID 11763309 | — |
| Reactant | 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-phenylcarbamoyl-uridine | HCID 44250652 | — |
| Catalyst | copper(II) trifluoromethanesulfonate | HCID 2734996 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3'-O-phenylcarbamoyl-uridine | HCID 66842597 | — |
Reaction Steps
The THF solution (1 ml) containing 3aR-[2(3′aR,8′aS),3′aβ,8′aβ]]-2,2′-methylenebis[3a,8a-dihydro-8H-indeno-[1,2-d]oxazole] (0.03 mmol, 10.1 mg) and Cu(OTf)2 (II) (0.03 mmol, 11.1 mg) was stirred for 30 minutes at room temperature. After the reaction mixture was cooled to 0° C., the THF solution (1.5 ml) of 5′-O-[bis(4-methoxyphenyl)phenylmethyl]uridine (0.3 mmol, 164.0 mg) and the THF solution (1 ml) of phenyl isocyanate (0.3 mmol, 35.7 mg) were added thereto. After the mixture was continuously stirred for 1 hour at 0° C. and for 1.5 hours at room temperature, the mixture was analyzed with high-performance liquid chromatography. As a result, it was found that 5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-phenylcarbamoyl-uridine and 5′-O-[bis(4-methoxyphenyl)phenylmethyl]-3′-O-phenylcarbamoyl-uridine were produced at the ratio of 82:18, and the transformation ratio of the reaction was 76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252919B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-a6d386dfdc6645fd887d0668ea99a6eb |
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| Source note | uspto-grants-2012_08 |
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