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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751250Generated: October 30, 2026

N-bromobutanimide → 5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

https://huagongshe.com/reaction/751250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5H-Pyrrolo3,2-dpyrimidin-2-amine, 4-(phenylmethoxy)-5-(phenylmethoxy)methyl-HCID 22222458—
SolventDichloromethaneHCID 6344—
Product5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-HCID 1181221294.3%

Reaction Steps

A solution of 2-amino-4-benzyloxy-5-N-benzyloxymethylpyrrolo[3,2-d]pyrimidine (1.0 g) in methylene chloride (30 mL) was stirred in an ice bath while N-bromosuccinimide (0.5 g) was added portion-wise. The solution was concentrated and chromatography afforded 2-amino-4-benzyloxy-5-N-benzyloxymethyl-7-bromopyrrolo[3,2-d]pyrimidine (1.15 g) as a white solid. 13C NMR (CDCl3), δ 158.8, 157.2, 150.9, 137.3, 136.6, 131.8, 129.0, 128.8, 128.6, 128.5, 128.3, 127.9, 111.3, 90.3, 77.8, 70.7, 68.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405297B2
Source datasetuspto-grants-2008_07
ORD IDord-62237af0ae3f4945b6fa774348d50f47
Source noteuspto-grants-2008_07