US PATENT SUBCLASS 540 / 504
.~.~.~.~.~.~ The bicyclo ring system is 1,4-benzodiazepine (including hydrogenated)


Current as of: June, 1999
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540 /   HD   ORGANIC COMPOUNDS -- PART OF THE CLASS 532-570 SERIES

*  DD  ORGANIC COMPOUNDS (Class 532, Subclass 1) {1}
1  DF  .~ HETEROCYCLIC CARBON COMPOUNDS CONTAINING A HETERO RING HAVING CHALCOGEN (I.E., OXYGEN, SULFUR, SELENIUM OR TELLURIUM) OR NITROGEN AS THE ONLY RING HETERO ATOMS {6}
484  DF  .~.~ The hetero ring contains seven members including nitrogen and carbon {14}
485  DF  .~.~.~ Chalcogen double bonded directly to a ring carbon adjacent to the ring nitrogen (e.g., caprolactam, etc.) {15}
492  DF  .~.~.~.~ Plural nitrogens in the hetero ring {3}
500  DF  .~.~.~.~.~ Bicyclo ring system having the hetero ring as one of the cyclos {4}
504.~.~.~.~.~.~ The bicyclo ring system is 1,4-benzodiazepine (including hydrogenated) {10}
505  DF  .~.~.~.~.~.~.~> The chalcogen double bonded directly to the hetero ring is sulfur
506  DF  .~.~.~.~.~.~.~> Additional chalcogen bonded directly to ring carbon of the hetero ring {1}
509  DF  .~.~.~.~.~.~.~> Acyclic nitrogen bonded directly to the hetero ring
510  DF  .~.~.~.~.~.~.~> Having -C(=X)-, wherein X is chalcogen, bonded directly to the hetero ring
511  DF  .~.~.~.~.~.~.~> Halogen bonded directly to the hetero ring
512  DF  .~.~.~.~.~.~.~> Chalcogen attached indirectly to nitrogen of the hetero ring by acyclic nonionic bonding
513  DF  .~.~.~.~.~.~.~> Sulfur, -C(=X)-, wherein X is chalcogen, or nitrogen, other than as nitro or nitroso, bonded directly to the carbocyclic ring of the bicyclo ring system
514  DF  .~.~.~.~.~.~.~> Nitrogen in the 1-position substituent of the bicyclo ring system
515  DF  .~.~.~.~.~.~.~> Preparation by cyclizing benzophenones or imine derivatives thereof
516  DF  .~.~.~.~.~.~.~> Preparation from a compound containing a different hetero ring


DEFINITION

Classification: 540/504

(under subclass 500) Compounds wherein the bicyclo ring system has the following structure, which may contain double bonds between its members [figure]

(1) Note. An example of a compound provided for herein is: [figure]