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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373890Generated: October 30, 2026

HCID 19808606, compound → HCID 19808645, compound

https://huagongshe.com/reaction/373890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19808606HCID 19808606—
SolventMethanol, 1,1-diethoxy-, 1-acetateHCID 84166—
ProductHCID 19808645HCID 1980864556%

Reaction Steps

A solution of 6-[[1-(t-butyldimethylsilyloxymethyl)-3-(diethoxyphosphoryl)propoxy]amino]-4-chloro-5-formamidopyrimidine (0.5 g) in diethoxymethyl acetate (5 ml) was heated at 110° C. for 2 hours. The solvent was evaporated under reduced pressure, the residue dissolved in methanol (5 ml) and 0.880 ammonia (0.1 ml) added. After 30 minutes at ambient temperature, the solvent was evaporated and the residue chromatographed on silica gel using dichloromethane-methanol (98:2) as eluant. This afforded the title compound (0.27 g, 56%) as a yellow oil. IR: υmax (film) 2940, 2870, 1595, 1565, 1440, 1390, 1340, 1250, 1220, 1060, 1030, 970, 930, 840, 790 cm-1. 1H NMR: δH (CDCl3) 0.0 (6H, s, SiMe2), 0.8 (9H, s, SiBut), 1.25 (6H, t, J=7Hz, (OCH2CH3)2), 1.8-2.4 (4H, m, CH2CH2P) 3.8 (2H, d, J=6Hz, CH2OSi), 4.1 (4H, m, (OCH2CH3)2), 4.6 (1H, m, CHON), 8.35 (1H, s), 8.75 (1H, s). Found: C, 45.97; H, 6.89; N, 10.80%. C19H34N4O5PSiCl requires: C, 46.28; H, 6.95; N, 11.36%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166198
Source datasetuspto-grants-1992_11
ORD IDord-2993c6ef46304033a81a36fd03e4e1f6
Source noteuspto-grants-1992_11