HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416388Generated: November 2, 2026
Ammonium formate → 5-[3-(2-Trifluoroacetamidoethoxy)propyl]2'-deoxyuridine
https://huagongshe.com/reaction/1416388
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 5-[3-(2-Trifluoroacetamidoethoxy)propynyl]-2'-deoxyuridine | HCID 21309568 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-[3-(2-Trifluoroacetamidoethoxy)propyl]2'-deoxyuridine | HCID 54422210 | 87% |
Reaction Steps
A solution of 5-[3-(2-trifluoroacetamidoethoxy)propynyl]-2'-deoxyuridine (3.4 g, 8.1 mmol) in methanol (20 ml) is stirred with ammonium formate (prepared by addition of 3 ml, 79 mmol of cold 98% formic acid into 2 ml, 50 mmol of dry ice frozen 25% ammonia) and 0.2 g of 10% Pd/C for 7 hours at room temperature under hydrogen atmosphere. The catalyst is removed by filtration, the filtrate evaporated and product is purified on LiChroprep RP-18 column by the above procedure. Fractions containing the desired product are combined and evaporated to dryness in vacuo and the resultant solid is triturated with dry ether to give 3.0 g (87% product, m.p. 107-110°; max in nm, in 0.1M triethylamine-acetate (pH 7.5), 220, 268. Analysis calculated for C16H22F3N3O7 : C, 45.18; H, 5.21; N, 9.88; F, 13.40. Found C, 45.16; H, 5.16; N, 9.68; F, 13.13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05912340 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-336d066d64ad4ab29d6f9a9e34e87817 |
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| Source note | uspto-grants-1999_06 |
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