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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264724Generated: November 1, 2026

Chlorotrimethylsilane → N2-Isobutyryl-2'-O-Methyl-guanosine

https://huagongshe.com/reaction/264724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium HydroxideHCID 14923—
ReactantIsobutyryl chlorideHCID 62325—
Reactant2'-O-MethylguanosineHCID 135406950—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductN2-Isobutyryl-2'-O-Methyl-guanosineHCID 135536008—

Reaction Steps

2'-O-methylguanosine (3.5 g) in pyridine (100 ml) was treated with trimethylsilyl chloride (9 ml, 6 eq) and isobutyryl chloride (6.2 ml) at RT for 4 hr. The reaction mixture was cooled in an ice bath, H2O (20 ml) was added and stirring continued for an additional 20 min. NH4OH (20 ml) was added and after stirring for 30 min the reaction mixture was evaporated. The residue was triturated with H2O, filtered and the filtrate evaporated and purified by silica gel chromatography as per the procedure of Example 4 to yield the product as an off white solid (1.5 g). 1H NMR (DMSO-d6) δ 1.1 [d, 6, CH(CH3)2 ], 2.77 [m, 1, CH(CH3)2 ], 3.33-3.6 (m, 5, OCH3, H-5'), 3.93 (m, 1, H-4'), 4.22 (m, 1), 4.3 (m, 1), 5.1 (t, 1, 5'-OH), 5.28 (d, 1, 3'-OH), 5.9 (d, 1, H-1'), 8.28 (s, 1, H-8) and 11.9 (br s, 1, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646265
Source datasetuspto-grants-1997_07
ORD IDord-a2e7812be4484ffcb67a8b0703ffb1e2
Source noteuspto-grants-1997_07