HCID 15068624, compound → HCID 20252039, compound

HRID 279870Notes

Reaction equation

HRID 279870 reaction equation
C(OC([N:11]1[CH2:16][CH:15]2[CH2:17][C:18]([Cl:21])([C:19]#[N:20])[CH:12]1[CH:13]=[CH:14]2)=O)C1C=CC=CC=1.C(O)(=O)C.[BrH:26]>C(O)(=O)C>[BrH:26].[Cl:21][C:18]1([C:19]#[N:20])[CH2:17][CH:15]2[CH:14]=[CH:13][CH:12]1[NH:11][CH2:16]2

Participants

4

Procedure

5.0 g. (0.0165 moles) of N-benzyloxycarbonyl-7-chloro-7-cyano-2-azabicyclo[2.2.2]oct-5-ene are dissolved in a mixture of 30 ml. of glacial acetic acid and 15 ml. of a 4-5N glacial acetic acid/hydrogen bromide mixture. The reaction mixture is allowed to stand at room temperature for 10 minutes, and is then evaporated. The evaporation residue is crystallized from acetone.

Workup

  1. customis then evaporated
  2. customThe evaporation residue is crystallized from acetone

Sources & evidence

ORD record
ord-e31874ef70ca481ba196f82b5c642d33
Source dataset
uspto-grants-1986_05
Patent number
US04587251

Reaction notes

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