HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Aminothiophene-2-sulfonamide → 4-[5-Bromo-4-(1-hydroxymethyl-propylamino)-pyrimidin-2-ylamino]-thiophene-2-sulfonic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Aminothiophene-2-sulfonamide | HCID 24711598 | — |
| Reactant | 4-Aminothiophene-2-sulfonamide | HCID 45080588 | — |
| Reactant | (R)-2-(2-chloro-5-bromopyrimidine-4-ylamino)butan-1-ol | HCID 58891316 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[5-Bromo-4-(1-hydroxymethyl-propylamino)-pyrimidin-2-ylamino]-thiophene-2-sulfonic acid amide | HCID 69332142 | — |
Reaction Steps
530 mg (1.9 mmol) of (R)-2-(5-bromo-2-chloro-pyrimidin-4-ylamino)-butan-1-ol is added to a suspension of 303 mg of a mixture that consists of 4-amino-thiophene-2-sulfonic acid amide and 5-amino-thiophene-2-sulfonic acid amide (ratio: 2:1) in 7 ml of ethanol and 170 μl of concentrated HCl. The reaction mixture is stirred for 21 hours under reflux. After cooling, the batch is purified by chromatography (Flashmaster II, hexane/EE 2:8). The crude product that is obtained is then recrystallized (ethyl acetate/diisopropyl ether). 47 mg (0.11 mmol, 7% of theory) of the product 4-[5-bromo-4-(1-hydroxymethyl-propylamino)-pyrimidin-2-ylamino]-thiophene-2-sulfonic acid amide is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07288547B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-2da2ba2ba2ef4b8289ee8b1b82d63104 |
| Source note | uspto-grants-2007_10 |