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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292595Generated: October 31, 2026

2',3',5'-tri-O-benzoyl-2-chloro-N-[(R)-1-(2-thiazolyl)thio-2-propyl]adenosine → Adenosine

https://huagongshe.com/reaction/2292595

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2',3',5'-tri-O-benzoyl-2-chloro-N-[(R)-1-(2-thiazolyl)thio-2-propyl]adenosineHCID 22858317—
SolventAmmoniaHCID 222—
ProductAdenosineHCID 6096179.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

2',3',5'-Tri-O-benzoyl-2-chloro-N-[(R)-1-(2-thiazolyl)thio-2-propyl]adenosine (1.2 g, 1.5 mmol) was dissolved in methanolic ammonia (25 ml) (previously saturated at -10° C.) and stirred at 20° C. for 40 h. The reaction mixture was concentrated to an oil at reduced pressure and purified by flash chromatography eluting with a mixture of dichloromethane, ethanol and ammonia (90:10:1), to provide the title 2-chloro-N-[(R)-1-(2-thiazolyl)thio-2-propyl)]adenosine (0.32 g, 46%) as a foam, 1H NMR (DMSO-d6) δ1.31 (3H, d, CHCH3), 3.95 (1H, q, H-4'), 4.12 (1H, q, H-3'), 4.51 (1H, q, H-2'), 5.07 (1H, t, 5'-OH), 5.22, 5.50 (2H, 2d, 2'-and 3'-OH), 5.82 (1H, d, H-1'), 7.63 (1H, d, Ar--H), 7.72 (1H, d, Ar--H), 8.41 (1H, s, H-8), 8.48 (1H, d, N--H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05683989
Source datasetuspto-grants-1997_11
ORD IDord-1dc76612260446b6b5c21297eafec1dd
Source noteuspto-grants-1997_11