Diisopropylcarbodiimide → (2-(1Azabicyclo[2.2.2]oct-3yl)acetoxy}-2,3,5,6-tetrafluorobenzoic acid

HRID 1896491Notes

Reaction equation

HRID 1896491 reaction equation
[OH:1][C:2]1[C:10]([F:11])=[C:9]([F:12])[C:5]([C:6]([OH:8])=[O:7])=[C:4]([F:13])[C:3]=1[F:14].Cl.[N:16]12[CH2:23][CH2:22][CH:19]([CH2:20][CH2:21]1)[CH:18]([CH2:24][C:25](O)=[O:26])[CH2:17]2.C(N=C=NC(C)C)(C)C>CN(C=O)C.CN(C1C=CN=CC=1)C>[N:16]12[CH2:21][CH2:20][CH:19]([CH2:22][CH2:23]1)[CH:18]([CH2:24][C:25]([O:1][C:2]1[C:3]([F:14])=[C:4]([F:13])[C:5]([C:6]([OH:8])=[O:7])=[C:9]([F:12])[C:10]=1[F:11])=[O:26])[CH2:17]2

Participants

6

Procedure

2 g of the polymeric support resin from Example 8A (loading about 1.36 mmol/g, 2.72 mmol) are suspended in 20 ml of DMF and shaken with 1.23 g (5.98 mmol) of 1-azabicyclo[2.2.2]oct-3-ylacetic acid hydrochloride and 130 mg (1.09 mmol) of DMAP for 10 min. Then 1.06 ml (6.80 mmol) of N,N′-diisopropylcarbodiimide are added, and the mixture is shaken overnight. The resin is filtered off with suction, washed twice each with 20 ml each of DMF, THF and DCM and dried under high vacuum. 2.318 g of the polymer-bound title compound are obtained.

Workup

  1. filtrationThe resin is filtered off with suction
  2. washwashed twice each with 20 ml each of DMF, THF and DCM
  3. customdried under high vacuum

Sources & evidence

ORD record
ord-4246ec0e320f479ba6feda3a69b9de48
Source dataset
uspto-grants-2013_08
Patent number
US08518967B2

Reaction notes

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