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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720543Generated: November 1, 2026

Chlorotrimethylsilane → HCID 135533268, compound

https://huagongshe.com/reaction/1720543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium HydroxideHCID 14923—
ReactantIsobutyryl chlorideHCID 62325—
ReactantHCID 135494296HCID 135494296—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 135533268HCID 135533268—

Reaction Steps

2'-O-Propylguanosine (3.6 gm) in pyridine (50 ml) was cooled in an ice bath and trimethylsilyl chloride (8.4 ml, 6 eq.) was added. The reaction mixture was stirred for 30 min and isobutyryl chloride (5.8 ml, 5 eq.) was added. The solution was stirred for 4 hours during which it was allowed to warm to room temperature. The solution was cooled, H2O added (10 ml) and the solution was stirred for an additional 30 mins. Concentrated NH4OH (10 ml) was added and the solution evaporated in vacuo. The residue was purified by silica gel chromatography using 10% MeOH/CH2CL2 to elute the product. Product-containing fractions were evaporated to yield 2.5 g of product as a foam. An analytical sample was re-chromatographed on silica and eluted with CH2Cl2 →6% MeOH/CH2Cl2. 1H NMR (DMSO-d6) δ 0.75 (t 3, CH3) 1.13 [d, 6, CH(CH3)2 ], 1.4 (m, 2, CH2), 2.75 [m, 1, CH(CH3)2 ], 3.52 (m, 6, OCH2), 3.36 and 3.6 (ABX, 2, H-5'), 3.95 (m, 1), 4.26 (m, 1), 4.33 (m, 1), 5.07 (t, 1, 5'-OH), 5.18 (d, 1, 3'-OH), 5.9 (d, 1, H-1'), 8.25 (s, 1, H-8), 11.65 (br s, 1, NH) and 12.1 (br s, 1, NH). Anal. Calcd. for C17H25N5O6.1/2H2O: C, 50.49; H, 6.48; N, 17.32. Found: C, 50.81; H, 6.62; N, 17.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506351
Source datasetuspto-grants-1996_04
ORD IDord-74d3064174304848be92c8f3714a2df6
Source noteuspto-grants-1996_04