226900-35-2Relevant articles and documents
Synthetic studies towards ML-3000: A concise synthesis of this non- steroidal anti-inflammatory drug
Cossy, Janine,Belotti, Damien
, p. 5145 - 5156 (2007/10/03)
ML-3000 was obtained from 1-chloro-3-phenyl-2-propyne in 8 steps with an overall yield of 19%. The key steps are a thermal acid-promoted bicyclization of an ω-acetylenic amino ester and a Suzuki cross-coupling reaction between a heteroaryl triflate and (4-chlorophenyl)boronic acid.