Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342918Generated: October 30, 2026

Triphenylphosphine → HCID 54131397, compound

https://huagongshe.com/reaction/342918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 13964206HCID 13964206—
ReactantHCID 178506933HCID 178506933—
SolventDimethylformamideHCID 6228—
ProductHCID 54131397HCID 54131397—

Reaction Steps

N6 -Benzoyl-9-(5-O-benzoyl-2-deoxy-β-D-threo-pentofuranosyl)adenine (7.0 g, 15.3 mmol), triphenylphosphine (6.0 g, 22.9 mmol), and LiN3 (2.8 g, 56.4 mmol) were dissolved in DMF (100 mL). To this stirring mixture was added diethylazodicarboxylate (3.6 mL, 22.9 mmol) in one portion, the reaction was stirred for 2.5 h at RT, and the reaction was quenched with H2O (10 mL). The solvents were removed in vacuo, the residual oil was redissolved in EtOAc (300 mL) and extracted with H2O (2×200 mL) and saturated. aq. NaCl (200 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residual oil was purified on SiO2 (2-5% MeOH/CH2Cl2) to afford 5'-O-Benzoyl-N2 -benzoyl-3'-azido-2',3'-dideoxyadenosine, 1a, as an amber foam, which was taken on directly to hydrogenation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859233
Source datasetuspto-grants-1999_01
ORD IDord-3ef0a14e99cc40ae920bf38dd7b4f8db
Source noteuspto-grants-1999_01