HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 6-chloro-N-(1,3-thiazol-2-yl)pyridine-3-sulfonamide | HCID 943191 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamide | HCID 57551221 | — |
Reaction Steps
6-Chloro-pyridine-3-sulfonic thiazol-2-ylamide (200 mg, 0.0007 mol) in 7 M of Ammonia in methanol (5.00 mL) was heated at 160° C. in a pressure bottle for ˜6 h. The reaction had to be stopped because the pressure was too high and some of the reaction solution was leaking. By LC/MS, reaction show ˜30% conversion. The reaction solution was concentrated and then purified on Gilson (Prep LC, reverse phase, Phenomenex 250×30 mm, 15 micron C18 column, 40 mL/min. Gradient, 85% A to 100% B over 25 min. Solvent A: 7800 water/200 acetonitrile/8 TFA. Solvent B: 7200 acetonitrile/800 water/8). Fractions were checked by LC/MS and dried on a lyophilizer to give the product as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124610B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-eb7f88e94a7e4f4c9256bf2800a20ad8 |
| Source note | uspto-grants-2012_02 |