HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(6-Bromothiazolo[5,4-b]pyridin-2-yl)benzamide | HCID 11002134 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine | HCID 44612774 | 98% |
Reaction Steps
A solution of N-(6-bromothiazolo[5,4-b]pyridin-2-yl)benzamide III (2.0 g, 5.98 mmol) in 70% H2SO4 (10.0 mL) was heated to 140° C. for 1 h. After the completion of the reaction (TLC monitoring), the reaction mixture was poured onto crushed ice, basified with 30% aqueous NaOH solution till pH 8.0 and extracted with EtOAc (3×150 mL). The combined organics was washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure to obtain the desired product (1.34 g, 98%). 1H NMR (400 MHz, DMSO-d6): δ 7.85 (d, J=2.0 Hz, 1H), 8.05 (br s, 2H) and 8.18 (d, J=2.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299065B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-17fc1aa22e424997bb1c4c379aafca86 |
| Source note | uspto-grants-2012_10 |