TY - JOUR
T1 - Formylation Reaction of Amines Using N-Formylcarbazole
AU - Kang, Bubwoong
AU - Shimizu, Yuki
AU - Tamura, Yusaku
AU - Fukuda, Eigo
AU - Hamamoto, Ken Ichiro
AU - Uchida, Yuichiro
AU - Yasuno, Yoko
AU - Nakayama, Atsushi
AU - Satoh, Tetsuya
AU - Kuse, Masaki
AU - Shinada, Tetsuro
N1 - Funding Information:
This work was financially supported by the Tenure Track Support Program of Kobe University (for Bubwoong Kang) and a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (JSPS KAKENHI, Grant No. JP21K14792 for Bubwoong Kang; No. JP20H02745 for Tetsuya Satoh and Tetsuro Shinada).
Publisher Copyright:
© 2022 The Pharmaceutical Society of Japan
PY - 2022/7/1
Y1 - 2022/7/1
N2 - Formamides are useful starting materials for pharmaceutical syntheses. Although various synthetic methods have been documented in this regard, the use of N-formylcarbazole as a formylation reagent for amines has not yet been reported. We report here the first examples of the use of N-formylcarbazole for the formylation of amines. The characteristic reactivity of N-formylcarbazole enables the selective formylation of sterically less hindered aliphatic primary and secondary amines. In contrast, sterically bulkier amines and weakly nucleophilic amines such as anilines are less reactive under the reaction conditions.
AB - Formamides are useful starting materials for pharmaceutical syntheses. Although various synthetic methods have been documented in this regard, the use of N-formylcarbazole as a formylation reagent for amines has not yet been reported. We report here the first examples of the use of N-formylcarbazole for the formylation of amines. The characteristic reactivity of N-formylcarbazole enables the selective formylation of sterically less hindered aliphatic primary and secondary amines. In contrast, sterically bulkier amines and weakly nucleophilic amines such as anilines are less reactive under the reaction conditions.
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U2 - 10.1248/cpb.c22-00161
DO - 10.1248/cpb.c22-00161
M3 - Article
C2 - 35786568
AN - SCOPUS:85133247677
SN - 0009-2363
VL - 70
SP - 492
EP - 497
JO - Chemical and Pharmaceutical Bulletin
JF - Chemical and Pharmaceutical Bulletin
IS - 7
ER -