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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729404Generated: October 30, 2026

Sodium hydride → HCID 131717242, compound

https://huagongshe.com/reaction/1729404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylateHCID 9906257—
Reactant6-Chloro-8-propyl-9H-purineHCID 19012223—
SolventDimethylformamideHCID 6228—
ProductHCID 131717242HCID 131717242—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a suspension of NaH (0.20 g) in dry DMF (3 ml), 6-chloro-8-propyl-purine (0.06 g, 0.3 mmol) was added, and the mixture was stirred at 40° C. for 20 minutes. t-Butyl-4-bromomethylbiphenyl-2'-carboxylate (0.11 g, 0.31 mmol) was then added at room temperature and stirring continued for 3 hours at 40° C. The content of the flask was poured into ice-water (100 ml and extracted with ethylacetate. The organic phase was separated and dried over MgSO4. Removal of the solvent under reduced pressure gave the crude product which was then purified by flash-chromatography on silica-gel using ethylacetate-hexane (1:1). The pure titled compound was obtained as a glass-like solid (0.073 g, 53%). NMR (CDCl3): δ 1.04 (t, J=9 Hz, 3H), 1.213 (s, 9H), 1.91 (m, 2H), 2.89 (t, 2H), 5.52 (s, 2H), 7.15-7.52 (m, 7H), 7.79 (dd, J1 =8 Hz and J2 =2 Hz, 1H), 8.72 (s, 1H); FAB-MS: m/e 463 and 465 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332744
Source datasetuspto-grants-1994_07
ORD IDord-ef65e44d4ee64f52967555881ac4f208
Source noteuspto-grants-1994_07