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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Carbonic acid, compound with phenylguanidine (1:1) | HCID 16217093 | — |
| Reactant | Tert-butyl 3-(3-trimethylsilylpropynoyl)pyrrolo[3,2-c]pyridine-1-carboxylate | HCID 58230463 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | phenyl[4-(1H-pyrrolo[3,2-c]pyridin-3-yl)pyrimidin-2-yl]-amine | HCID 24884486 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293891B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-0ca1724f31414102b60586fa4f270013 |
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| Source note | uspto-grants-2012_10 |
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