HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063771Generated: November 1, 2026
Triethylamine → 5-Bromo-3',5'-diacetyl-N4-(2-hydroxy-m-nitrophenyl)-2'-deoxycytidine
https://huagongshe.com/reaction/1063771
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-Amino-4-Nitrophenol | HCID 3613389 | — |
| Reactant | HCID 22854693 | HCID 22854693 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-3',5'-diacetyl-N4-(2-hydroxy-m-nitrophenyl)-2'-deoxycytidine | HCID 69743624 | — |
Reaction Steps
To a solution of 3′,5′-diacetyl-5-bromo-2′-deoxyuridine (4.8 g; 12 mmol), methylene chloride (50 ml), triethylamine (5.0 g; 50 mmol) and DMAP (0.10 g) was added 2-mesitylsulfonyl chloride (5.2 g; 24 mmol). After stirring at room temperature for 4 h., DBU (3.6 g; 24 mmol) and 2-amino-4-nitrophenol (7.4 g; 48 mmol) were added and the solution was stirred for 3 h. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and saturated sodium bicarbonate. The organic layer was purified by flash column chromatography on silica gel. The isolated product had some impurity and was triturated with ethyl acetate. The yellowish precipitate was filtered off and washed with methylene chloride to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06967079B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-85e9a7c1058d43f48801f4d37b0b3d19 |
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| Source note | uspto-grants-2005_11 |
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