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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281505Generated: November 3, 2026

Water → HCID 86636624, compound

https://huagongshe.com/reaction/2281505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant1-BOC-3-AminopiperidineHCID 545809—
Reactant2,4-dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidineHCID 53486828—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86636624HCID 8663662472.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,4-dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine (233 mg, 0.681 mmol), 3-amino-1-N-Boc-piperidine (136 mg, 0.680 mmol) and TEA (0.200 mL, 1.44 mmol) in dioxane (5 mL) was stirred at 70° C. for 20 h. Water and EtOAc were added. The organic phase was separated, washed with 1N HCl, then with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo to give tert-butyl 3-(2-chloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)piperidine-1-carboxylate (251 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139581B2
Source datasetuspto-grants-2015_09
ORD IDord-09705b57b1e24446a383677fbfb9edf7
Source noteuspto-grants-2015_09