FIELD: medical chemistry.
SUBSTANCE: method for producing a cyclic alkylene urea product of Formula I:
wherein a compound of Formula II and/or Formula III is contacted in a reaction zone with a compound of Formula IV and/or Formula V and in the presence of one or more carbonyl-delivering compounds,
in which R1 represents -[AX-]qR3; R2 in each case is independently selected from H and C1 to C6 alkyl groups, which are optionally substituted by one or two groups selected from -OH and -NH2; R3 in each case is independently selected from H and C1 to C6 alkyl groups, which are optionally substituted by one or two groups selected from -OH and -NH2 ; A is in each instance independently selected from C1 to C3 alkylene units, optionally substituted with one or more C1 to C3 alkyl groups; X is in each case independently selected from -O-, -NR2-, a group of Formula VI and a group of Formula VII:
,
and p and q are each independently selected from an integer in the range 0-8. In this case, a compound of Formula II and/or a compound of Formula III is added to the reaction zone containing a compound of Formula IV and/or a compound of Formula V, continuously, semi-continuously or in two or more batches, and the carbonyl-delivering compound contains a carbonyl group transferred to the alkanolamine or alkylenediamine compound to form, respectively, a cyclic alkylene carbamate or a cyclic alkylene urea.
EFFECT: improved overall conversions and/or improved selectivity.
12 cl, 1 dwg, 5 tbl, 6 ex
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Authors
Dates
2023-09-26—Published
2018-08-07—Filed