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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenamine, 3-ethynyl- | HCID 104682 | — |
| Reactant | 4-Chloro-5-(methylsulfanyl)-7H-pyrrolo[2,3-D]pyrimidine | HCID 10774384 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Ethynyl-phenyl)-(5-methylsulfanyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amine | HCID 22460823 | 27.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06395733B1 |
|---|
| Source dataset | uspto-grants-2002_05 |
|---|
| ORD ID | ord-e36e440249db48d89ffb603570f5d4eb |
|---|
| Source note | uspto-grants-2002_05 |
|---|