HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089417Generated: October 31, 2026
1-Methylimidazole → 5'-Deoxy-5-fluorocytidine
https://huagongshe.com/reaction/1089417
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2',3'-di-O-benzoyl-5'-deoxy-5-fluorouridine | HCID 12135357 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5'-Deoxy-5-fluorocytidine | HCID 10037499 | — |
Reaction Steps
To a mixture of N-methylimidazole (0.8 ml) and phosphoryl chloride (0.28 ml) in acetonitrile (20 ml) was added 2',3'-di-O-benzoyl-5'-deoxy-5-fluorouridine (500 mg) obtained above at 0° C. After stirring of the reaction mixture for 1.5 hours at room temperature 28% ammonium hydroxide (2.5 ml) was added to the mixture at 0° C., and the mixture was stirred for 1 hour at room temperature. Acetonitrile and ammonia were removed under reduced pressure. The residue was acidified with 1N-HCl and then extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate to give 155 mg of 2',3'-di-O-benxoyl- 5'-deoxy-5-fluorocytidine, mp 192°~194° C.; MS 476 ((M+Na)+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04966891 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-26fa1d2236fd4819a2298b048de21c8d |
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| Source note | uspto-grants-1990_10 |
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