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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067706Generated: October 25, 2026

Water → phenyl[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)pyrimidin-2-yl]-amine

https://huagongshe.com/reaction/2067706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantCarbonic acid, compound with phenylguanidine (1:1)HCID 16217093—
ReactantTert-butyl 3-(3-trimethylsilylpropynoyl)pyrrolo[3,2-c]pyridine-1-carboxylateHCID 58230463—
Solvent2-MethoxyethanolHCID 8019—
Productphenyl[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)pyrimidin-2-yl]-amineHCID 24884486—

Reaction Conditions

Temperature40 °C

Reaction Steps

1.2 104 mg (0.75 mmol) of potassium carbonate are added to a solution of 103 mg (0.30 mmol of tert-butyl 3-(3-trimethylsilylpropynoyl)pyrrolo-[3,2-c]pyridine-1-carboxylate and 148 mg (0.75 mmol) of phenylguanidine carbonate in 1.5 ml of ethylene glycol monomethyl ether, and the mixture is heated at the boil for 68 hours. After cooling, 10 ml of water are added, and the mixture is stirred at 40° C. for 1 h. The precipitate formed is filtered off with suction, washed with water and dried in vacuo, giving phenyl-[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)pyrimidin-2-yl]amine (“A1”) as pale-brown solid; ESI 287;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293891B2
Source datasetuspto-grants-2012_10
ORD IDord-0ca1724f31414102b60586fa4f270013
Source noteuspto-grants-2012_10