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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720550Generated: October 31, 2026

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

https://huagongshe.com/reaction/1720550

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) 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 numberUS05506351
Source datasetuspto-grants-1996_04
ORD IDord-4c63ab59874e4a16b5c9a6b7a1a98cc4
Source noteuspto-grants-1996_04