USRE29195EExpiredUtility

7-(3-Chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane and its preparation

Priority: Oct 23, 1973Filed: Dec 8, 1975Granted: Apr 26, 1977
Est. expiryOct 23, 1993(expired)· nominal 20-yr term from priority
C07D 487/18
23
PatentIndex Score
2
Cited by
1
References
4
Claims

Abstract

.[.7-.]..Iadd.3.Iaddend.-Cis- or .[.7.]..Iadd.3.Iaddend.-cis-trans-(3-Chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane.[.-3-methanol.]. is prepared by reacting cis-, or cis-trans-.[.7.]..Iadd.1.Iaddend.-(3-chloro-2-propenyl)-3,5,7-triaza-1-azoniatricyclo(3.3.1.1 3 ,7)decane chloride with excess aqueous strong base at room temperature to give the corresponding .[.carbinolamine, 7-.]..Iadd.3.Iaddend.-(3-chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane.[.-3-methanol.]..

Claims

exact text as granted — not AI-modified
1.  A member of the group consisting of .[.7-.]. .Iadd.3-.Iaddend.cis-(3-chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)-nonane.[.-3-methanol.]. and .[.7-.]. .Iadd.3-.Iaddend.cis-trans-(3-chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane.[.-3-methanol.].. 
     
     
       2. .[.7-.]. .Iadd.3-.Iaddend.Cis-(3-chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane.[.-3-methanol.].. 
     
     
       3. .[.7-.]. .Iadd.3-.Iaddend.Cis-trans-(3-chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane.[.-3-methanol.].. 
     
     
       4. A method for making a .Iadd.3-.Iaddend.cis- or a mixture of .Iadd.3-.Iaddend.cis- and trans- .[.7-.]. -(3-chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane .[.-3-methanol.]. which comprises reacting at room temperature cis- or cis-trans- 1-(3-chloro-2-propenyl)-3,5,7-triaza-1-azoniatricyclo(3.3.1.1 3 ,7)-decane chloride with excess aqueous strong base and recovering the respective product .[.7-.]. .Iadd.3-.Iaddend.(3-chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1)nonane.[.-3-methanol.]. from the reaction medium.

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