HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391120Generated: November 1, 2026
6-(4-Methanesulfonyl-piperazin-1-ylmethyl)-2-methylsulfanyl-4-morpholin-4-yl-thieno[2,3-d]pyrimidine → 4-(6-((4-(Methylsulfonyl)piperazin-1-yl)methyl)-2-(5-phenylpyridin-3-yl)thieno[2,3-d]pyrimidin-4-yl)morpholine
https://huagongshe.com/reaction/391120
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-(4-Methanesulfonyl-piperazin-1-ylmethyl)-2-methylsulfanyl-4-morpholin-4-yl-thieno[2,3-d]pyrimidine | HCID 66617586 | — |
| Reactant | 3-Phenyl-5-tributylstannanyl-pyridine | HCID 66933870 | — |
| Catalyst | Bromo(thiobis(methane))copper | HCID 2724234 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(6-((4-(Methylsulfonyl)piperazin-1-yl)methyl)-2-(5-phenylpyridin-3-yl)thieno[2,3-d]pyrimidin-4-yl)morpholine | HCID 24945992 | — |
Reaction Steps
To a solution of 6-(4-methanesulfonyl-piperazin-1-ylmethyl)-2-methylsulfanyl-4-morpholin-4-yl-thieno[2,3-d]pyrimidine (135 mg) in 1,2-dimethoxyethane (10 mL) was added 3-phenyl-5-tributylstannanyl-pyridine (270 mg) and copper(I)bromide-dimethyl sulfide (125 mg) and the reaction mixture was stirred at room temperature for 10 minutes. Tetrakis(triphenylphosphine)palladium(0) (18 mg) was then added and the reaction mixture was heated at reflux for 16 h. After cooling to room temperature, the mixture was diluted with ethyl acetate (20 mL) and washed with water (2×20 mL) and brine (2×20 mL). The organic phase was dried (MgSO4), reduced in vacuo and purified by column chromatography to give 403. NMR: (CDCl3): 3.17 (3 H, s, Me), 3.93-3.95 (4 H, m), 4.13-4.16 (4 H, m), 5.28 (2 H, s, NH), 7.83 (1 H, t, J 7.0, Ar), 7.92 (1 H, s, Ar), 8.26 (2 H, td, J 7.7 and 1.5, Ar), 8.53-8.54 (1 H, m, Ar) and 9.30 (2 H, s, Ar). MS: (ESI+): MH+ 497.08
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383620B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-38409df1c1584a3093e47e88d1e71aa9 |
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| Source note | uspto-grants-2013_02 |
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