HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092598Generated: November 1, 2026
1-Butanesulfonyl chloride → HCID 68253359, compound
https://huagongshe.com/reaction/2092598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanesulfonyl chloride | HCID 75430 | — |
| Reactant | HCID 67329109 | HCID 67329109 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 68253359 | HCID 68253359 | 79% |
Reaction Steps
To a solution [6-(5-Amino-2-methyl-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine (50.0 mg, 0.116 mmol) in Pyridine (1 ml) at 0° C. was added Butane-1-sulfonyl chloride (21.3 mg, 0.139 mmol) dropwise The reaction mixture was stirred for 15 minutes at 0° C. and then allowed to attain room temperature. It was then further stirred for 3 hours at room temperature. The reaction mixture was concentrated under vacuum. The reaction mass was then, diluted with water and extracted with dichloromethane. The dichloromethane layer was washed with water, then with brine solution. The organic layer is dried over sodium sulphate and concentrated under reduced pressure. The crude product obtained was purified by column chromatography (SiO2, 2-10% methanol in chloroform) to give 50.4 mg (78.9%) Butane-1-sulfonic acid (4-methyl-3-{2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-6-yl}-phenyl)-amide [49] as off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440679B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-f4c0a9fc4537437d83beb22e1e3d207c |
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| Source note | uspto-grants-2013_05 |
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