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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937411Generated: October 25, 2026

Benzenamine, 3-ethynyl- → (3-Ethynyl-phenyl)-(5-methylsulfanyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amine

https://huagongshe.com/reaction/1937411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3-ethynyl-HCID 104682—
Reactant4-Chloro-5-(methylsulfanyl)-7H-pyrrolo[2,3-D]pyrimidineHCID 10774384—
SolventMethanolHCID 887—
Product(3-Ethynyl-phenyl)-(5-methylsulfanyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amineHCID 2246082327.1%

Reaction Conditions

Temperature125 °C

Reaction Steps

To 4-chloro-5-methylsulfanyl-7H-pyrrolo[2,3-d]pyrimidine (150 mg, 0.75 mmol) in dry methanol (2 ml) was added m-aminophenyl acetylene (110 mg, 0.90 mmol). The solution was heated in a sealed pressure tube at 125° C. for 5.5 hours. The reaction mixture was cooled to ambient temperature, filtered with a small amount of methanol and dried in vacuo to afford the title compound as a tan powder (57 mg, 27%). TS-MS: 281 (MH+); anal. RP18-HPLC RT:4.74 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395733B1
Source datasetuspto-grants-2002_05
ORD IDord-e36e440249db48d89ffb603570f5d4eb
Source noteuspto-grants-2002_05