4-Aminopyridine → HCID 13534274, compound

HRID 364950Notes

Reaction equation

HRID 364950 reaction equation
[O:1]=[C:2]1[N:9]2[C:5]([CH2:11][CH2:12][C:13]([OH:15])=O)([CH2:6][CH2:7][C:8]2=[O:10])[CH2:4][CH2:3]1.C1(N=C=NC2CCCCC2)CCCCC1.[NH2:31][C:32]1[CH:37]=[CH:36][N:35]=[CH:34][CH:33]=1>CN(C)C1C=CN=CC=1.C(Cl)Cl>[N:35]1[CH:36]=[CH:37][C:32]([NH:31][C:13](=[O:15])[CH2:12][CH2:11][C:5]23[CH2:6][CH2:7][C:8](=[O:10])[N:9]2[C:2](=[O:1])[CH2:3][CH2:4]3)=[CH:33][CH:34]=1

Participants

6

Reactant 3

HCID 17274-AminopyridineHCID 10868DicyclohexylcarbodiimideHCID 13306700HCID 13306700, compound

Product 1

HCID 13534274HCID 13534274, compound

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 6344DichloromethaneSolvent

Procedure

A suspension of 21.1 g of tetrahydro-3,5-dioxo-1H-pyrrolizine-7a(5H)-propanoic acid, 21.7 g of dicyclohexylcarbodiimide, and 100 mg of 4-dimethylaminopyridine (catalyst) in 100 ml of methylene chloride are treated with 9.4 g of 4-aminopyridine. The mixture is stirred for 16 hours and the by-product, N,N1 -dicyclohexylurea, is removed by filtration. The product is purified by chromatography over silica gel using 40% 2-propanol-methylene chloride for elution. After recrystallization from water, the product is isolated as a white solid with a melting point of 285°-287° C.

Workup

  1. customthe by-product, N,N1 -dicyclohexylurea, is removed by filtration
  2. customThe product is purified by chromatography over silica gel using 40% 2-propanol-methylene chloride for elution
  3. customAfter recrystallization from water
  4. customthe product is isolated as a white solid with a melting point of 285°-287° C.

Sources & evidence

ORD record
ord-14ead00063614cf7a4d9ca099e9cdedb
Source dataset
uspto-grants-1986_08
Patent number
US04607043

Reaction notes

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