Process for the preparation of monofunctionalized cyclic tetrami

Organic compounds -- part of the class 532-570 series – Organic compounds – Unsubstituted hydrocarbyl chain between the ring and the -c-...

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C07D25702

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050475274

ABSTRACT:
Process for the preparation of monofunctionalized cyclic tertramines of formula I ##STR1## in which R denotes a saturated or unsaturated, especially polymerizable, organic radical, characterized in that the corresponding tetraazacycloalkane compound (according to formula II) is prepared, in which three of the four nitrogen atoms are bonded via covalent bonds with a single atom or group of intracyclic atoms A, in that this triprotected compound is reacted with an organic compound RX (of formula III), X denoting a nucleophobic group, and in that the tetraazacycloalkane compound which is tri-protected and monofunctionalized on the unprotected nitrogen (according to formula IV) thus obtained is deprotected.

REFERENCES:
Chemical Abstract No. 85658a, vol. 96, No. 11, (Mar. 1982), p. 600.
Bouvier et al., Synth. React. Inorg. Met.-Org. Chem., "Synthesis and Characterization of Cyclamphosphate Sulfide and Selenide", vol. 17, No. 3, (1987), pp. 301-306.
Atkins et al., Tetrahedron Letters, "Polyaminophosphoranes III. P(III)-P(V) Tautomerism in Four Nitrogen Cage Phosphoranes", No. 52, (1978), pp. 5149-5152.
Dupart et al., Journal of the American Chemical Society, "Coordination Chemistry of Cyclamphosphorane, Access to Transition-Metal Cyclamphosphoranides, Crystal and Molecular Structure of CpMo(CO)2(Cyclamphosphoranide", vol. 108, No. 6 (Mar. 1986), pp. 1167-1173.
Chemical Abstract No. 69559j, vol. 107, No. 8, (1987).
French Search Report, Application No. FR 8903600.

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