HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391102Generated: October 28, 2026
2-Phenyl-5-tributylstannanyl-pyridine → 4-(6-((4-(Methylsulfonyl)piperazin-1-yl)methyl)-2-(6-phenylpyridin-3-yl)thieno[2,3-d]pyrimidin-4-yl)morpholine
https://huagongshe.com/reaction/391102
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Phenyl-5-tributylstannanyl-pyridine | HCID 14690011 | — |
| Reactant | 6-(4-Methanesulfonyl-piperazin-1-ylmethyl)-2-methylsulfanyl-4-morpholin-4-yl-thieno[2,3-d]pyrimidine | HCID 66617586 | — |
| 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-(6-phenylpyridin-3-yl)thieno[2,3-d]pyrimidin-4-yl)morpholine | HCID 24946534 | — |
Reaction Steps
To a solution of 6-(4-methanesulfonyl-piperazin-1-ylmethyl)-2-methylsulfanyl-4-morpholin-4-yl-thieno[2,3-d]pyrimidine (90 mg) in 1,2-dimethoxyethane (10 mL) was added 2-phenyl-5-tributylstannanyl-pyridine (180 mg) and copper(I)bromide-dimethyl sulfide (84 mg) and the reaction mixture was stirred at room temperature for 10 minutes. Tetrakis(triphenylphosphine)palladium(0) (12 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 387. NMR: (CDCl3): 2.65-2.69 (4 H, m), 2.82 (3 H, s, Me), 3.28-3.32 (4 H, m), 3.84 (2 H, s, CH2), 3.90-3.93 (4 H, m), 4.00-4.02 (4 H, m), 7.18 (1 H, s, Ar), 7.45-7.53 (3 H, m, Ar), 7.85 (1 H, d, J 8.5, Ar), 8.09-8.12 (2 H, m, Ar), 8.76 (1 H, d, J 8.5, Ar) and 9.72 (1 H, d, J 1.2, Ar). MS: (ESI+): MH+ 551.14
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-285d2ffa317448dd993dc9651770cb81 |
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| Source note | uspto-grants-2013_02 |
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