Singh, Harjit published the artcileSynthesis of heterocyclics via enamines. II. Reactions of cyclohex-1-enyl -aniline, -morpholine, and -piperidine with 1,1-dimethyl-3-oxobutyl isothiocyanate, Synthetic Route of 14294-10-1, the publication is Australian Journal of Chemistry (1975), 28(1), 143-9, database is CAplus.
The condensation of cyclohex-1-enylaniline with 1,1-dimethyl-3-oxobutyl isothiocyanate (I) gave mainly 1,5-benzodiazocine-6(1H)-thione II with some pyrimidine-2-thione III as the minor product. Similar condensations of I with cyclohex-1-enylmorpholine and cyclohex-1-enylpiperidine formed the 1-thiocarbamoyl derivatives through β-elimination of the intermediate IV (X = O, CH2).
Australian Journal of Chemistry 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 C10H16Br3N, Synthetic Route of 14294-10-1.
Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics