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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022425Generated: October 28, 2026

Hydrochloric Acid → HCID 135741792, compound

https://huagongshe.com/reaction/1022425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant2,4-Dichloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidineHCID 25230953—
ProductHCID 135741792HCID 135741792100.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

2,4-dichloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine (2.39 g, 11.8 mmol) was treated with a 2M aqueous potassium hydroxide solution (70 mL, 140 mmol). The reaction was warmed to 100° C., where it was stirred overnight. The reaction was allowed to cool down to room temperature gradually, where it stirred for an additional 2 nights. The reaction was brought to pH ˜7-8 with a 3N aqueous hydrochloric acid solution. The resulting light yellow mixture was cooled in an ice/water bath and filtered, rinsing twice with a small amount of water. The filtrate was brought to pH ˜2-3 with additional 3N aqueous hydrochloric acid solution. The resulting opaque light yellow mixture was filtered through the original filter cake. The solids were dried in vacuo to afford 2-chloro-7-methyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one as an off-white solid (2.18 g, 100%). NMR (300 MHz, DMSO-d6) δ ppm 3.67 (s, 3H) 6.46 (d, J=3.39 Hz, 1H) 7.11 (d, J=3.39 Hz, 1H) 12.83 (br. s., 1H). LC-MS calcd. for C7H7ClN3O [(M+H)+] 184, obsd, 183.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722661B2
Source datasetuspto-grants-2014_05
ORD IDord-754112e1d90a4c8ab0737fe544d130fb
Source noteuspto-grants-2014_05