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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751251Generated: November 1, 2026

Sodium hydride → HCID 22222449, compound

https://huagongshe.com/reaction/751251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-HCID 11812212—
SolventDimethylformamideHCID 6228—
ProductHCID 22222449HCID 22222449—

Reaction Steps

Sodium hydride (0.6 g, 50% dispersion) was added to a stirred solution of 2-amino-4-benzyloxy-5-N-benzyloxymethyl-7-bromopyrrolo[3, 2-d]pyrimidine (1.2 g) in N,N-dimethylformamide (25 mL) followed by 4-methoxybenzyl chloride (1.1 mL). After 1 h the reaction was quenched carefully with water, chloroform was added and the solution was washed (×2) with water. Normal processing followed by chromatography afforded 4-benzyloxy-5-N-benzyloxymethyl-7-bromo-2-{N,N-bis-(4-methoxybenzyl)amino}pyrrolo[3,2-d]pyrimidine (1.7 g) as a white solid. 13C-NMR (CDCl3), δ 159.0, 158.5, 156.5, 151.5, 137.4, 137.0, 131.8, 131.6, 129.7, 128.9, 128.8, 128.4, 128.3, 128.0, 114.1, 110.5, 91.1, 77.8, 70.6, 68.0, 55.7, 49.4. Anal. calc. for C37H35BrN4O4: C, 65.39; H, 5.19; Br, 11.76; N, 8.24. Found: C, 65.47; H, 5.17; Br, 11.55; N, 8.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405297B2
Source datasetuspto-grants-2008_07
ORD IDord-a3bc46109bb847dc95b63cb64fbd216d
Source noteuspto-grants-2008_07