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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456848Generated: October 30, 2026

N-bromobutanimide → HCID 69651329, compound

https://huagongshe.com/reaction/1456848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium AcetateHCID 517045—
Reactant60129-59-1HCID 3006222—
SolventDimethylformamideHCID 6228—
ProductHCID 69651329HCID 69651329—

Reaction Steps

NBS (1.42 g, 8.0 mmol, dissolved in 4 ml of dried DMF) is added, at room temperature, to a solution of 2'-deoxytubercidin (1.0 g, 4.0 mmol) and NaOAc (0.78 g, 8.0 mmol) in dried DMF (10 ml). The red solution is stirred for 10 minutes and then evaporated. Title compound (38) is obtained as colorless crystals (400 mg, 25%) following flash chromatography (column: 20-5 cm, CH2Cl2 /MeOH, 9:1), evaporation of the more rapidly migrating zone and subsequent recrystallization from isopropanol. Isolation of the more slowly migrating zone yields 5-bromo-2'-deoxytubercidin (130 mg, 10%). Method B: a solution of NBS (1.42 g, 8.0 mmol, dissolved in 4 ml of dried DMF) is added to a solution of 5-bromo-2'-deoxy-tubercidin (1.3 g, 4.0 mmol) and NaOAc (0.785 g, 8.0 mmol) in dried DMF (10 ml). Purification, see method A. Yield: 490 mg, 30% of 21. Melting point: 181° C. TLC (silica gel, CH2 Cl2 /MeOH, 9:1): Rf 0.40. 1H-NMR (D6 -DMSO): δ=2.12 (m, Hα -2'); 2.50 (m, Hβ -2'); 3.51 (m, 2H, H-5'); 3.84 (m, 1H, H-4'); 4.44 (m, 1H, H-3'); 5.20, (br, 2H, 5'-OH, 3'-OH); 6.42 ("t", J=6.2 Hz, 1H, H-1'); 6.93 (br, 2H, NH2); 8.10 (s, 1H, H-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05844106
Source datasetuspto-grants-1998_12
ORD IDord-01852c15bfd941318724a09f87a040cc
Source noteuspto-grants-1998_12