Kutschy, P. published the artcileReactivity of N’-substituted N-(4-pentynoyl)- and N-[2-(2-propynyl)-4-pentynoyl]thioureas, Category: amides-buliding-blocks, the publication is Chemical Papers (1987), 41(4), 519-26, database is CAplus.
Treatment of HCCCH2CHRCONHCSNR1R2 (I; R = H, HCCCH2; R1, R2 = H, Ph; R1R2N = morpholino) with EtONa and HgCl2 or Hg(OAc)2 resp., results in splitting-off the acyl residue and formation of H2NCSNR1R2. Heating I (R = HCCCH2, R1R2N = morpholino) EtOH with a catalytic amount of TiCl3 gave 58% (HCCCH2)2CHCONHCSOEt. Treating I (R = H, HCCCH2; R1 = R2 = Ph) with Br2 in CHCl3 gave 80-87% the benzothiazoline derivatives II (R = H, HCCCH2).
Chemical Papers published new progress about 14294-10-1. 14294-10-1 belongs to amides-buliding-blocks, auxiliary class Morpholine,Thiourea,Amine,Amide, name is Morpholine-4-carbothioamide, and the molecular formula is C5H10N2OS, Category: amides-buliding-blocks.
Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics