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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920662Generated: October 25, 2026

Hydrochloric Acid → N-Butyl-5H-pyrrolo[3,2-d]pyrimidin-2-amine

https://huagongshe.com/reaction/920662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButylamineHCID 8007—
Reactant2-Chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 45789986—
SolventIsopropanolHCID 3776—
ProductN-Butyl-5H-pyrrolo[3,2-d]pyrimidin-2-amineHCID 8673115496%

Reaction Conditions

Temperature170 °C

Reaction Steps

A suspension of 2-chloro-5H-pyrrolo[3,2-d]pyrimidine (0.62 g, 4 mmol) in 5 mL iPrOH was added nBuNH2 (2.5 mL, 25.3 mmol) and followed by HCl (2.0 mL, 4.0 M in dioxanes, 8 mmol). The resulting solution was heated at 170° C. for 1 h under microwave irradiation. The reaction was monitored by LC-MS. The reaction time should be extended whenever it is necessary. After evaporation of solvents, the crude product was washed with minimal amount of MeOH. The solid was collected. And the MeOH filtrate was purified by ISCO to provide the desired product (0.73 g, 96%). 1H NMR (400 MHz, CD3OD) δ 8.42 (d, J=0.8 Hz, 1H), 7.53 (d, J=3.1 Hz, 1H), 6.27 (dd, J=3.0, 0.8 Hz, 1H), 3.37 (t, J=7.1 Hz, 2H), 1.68-1.57 (m, 2H), 1.52-1.36 (m, 2H), 0.97 (t, J=7.4 Hz, 3H); MS m/z 191.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273056B2
Source datasetuspto-grants-2016_03
ORD IDord-2c45cc994563467b8e682c133669308f
Source noteuspto-grants-2016_03