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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362318Generated: October 31, 2026

5-(4-Benzyloxy-3-methoxyphenyl)-7-[3-(2-chloro-1-ethoxy)phenyl]-4-aminopyrrolo-[2,3-d]pyrimidine → 5-(4-Benzyloxy-3-methoxyphenyl)-7-[3-(2-(1-imidazolyl)ethoxy)phenyl]-4-amino-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/362318

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Benzyloxy-3-methoxyphenyl)-7-[3-(2-chloro-1-ethoxy)phenyl]-4-aminopyrrolo-[2,3-d]pyrimidineHCID 54542138—
ReactantHCID 178507081HCID 178507081—
SolventDimethylformamideHCID 6228—
Product5-(4-Benzyloxy-3-methoxyphenyl)-7-[3-(2-(1-imidazolyl)ethoxy)phenyl]-4-amino-pyrrolo[2,3-d]pyrimidineHCID 53687208—

Reaction Steps

0.8 g of 5-(4-benzyloxy-3-methoxyphenyl)-7-[3-(2-chloro-1-ethoxy)phenyl]-4-aminopyrrolo-[2,3-d]pyrimidine and 0.2 g of imidazolyl sodium are heated to 80° C. in 30 ml of DMF and the mixture is stirred for 5 h. It is then cooled to RT and concentrated. After chromatography on silica gel, 5-(4-benzyloxy-3-methoxyphenyl)-7-[3-(2-(1-imidazolyl)ethoxy)phenyl]-4-aminopyrrolo[2,3-d]pyrimidine having an m.p. of 122°-124° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869485
Source datasetuspto-grants-1999_02
ORD IDord-9a01d4518b5e418f85b0dfca66e98ef7
Source noteuspto-grants-1999_02