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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51516Generated: October 29, 2026

2-Morpholinoethylamine → 3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl N-(2-morpholinoethyl)carbamate

https://huagongshe.com/reaction/51516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethylamineHCID 408285—
Reactant3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl (4-nitrophenyl) carbonateHCID 86589008—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl N-(2-morpholinoethyl)carbamateHCID 22736269—

Reaction Steps

3-[4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl (4-nitrophenyl) carbonate (0.052 mmol) in dichloromethane (1 ml) was added to 2-morpholinoethylamine (0.2 ml). The resulting mixture was stirred under nitrogen at ambient temperature for 24 hours. The reaction mixture was diluted with ethyl acetate and washed, dried (MgSO4), filtered and evaporated. The solid was purified by preparative HPLC to give 3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl N-(2-morpholinoethyl)carbamate. The structure was confirmed by 1H NMR and LC/MS (MH+=543).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713474B2
Source datasetuspto-grants-2004_03
ORD IDord-cc1bc1fae08b4d8aadddb61f585bbd77
Source noteuspto-grants-2004_03