HCID 86748357, compound → HCID 18925459, compound

HRID 1077920Notes

Reaction equation

HRID 1077920 reaction equation
[C:1]([C:4]1[CH:34]=[CH:33][C:7]([C:8]([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]2[C:16]([N:18]2[CH2:23][CH2:22][CH:21]([O:24][CH2:25][C:26]([O:28]C(C)(C)C)=[O:27])[CH2:20][CH2:19]2)=[O:17])=[O:9])=[CH:6][CH:5]=1)(=[NH:3])[NH2:2]>ClCCl>[C:1]([C:4]1[CH:5]=[CH:6][C:7]([C:8]([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]2[C:16]([N:18]2[CH2:23][CH2:22][CH:21]([O:24][CH2:25][C:26]([OH:28])=[O:27])[CH2:20][CH2:19]2)=[O:17])=[O:9])=[CH:33][CH:34]=1)(=[NH:2])[NH2:3]

Participants

3

Reactant 1

HCID 86748357HCID 86748357, compound

Product 1

HCID 18925459HCID 18925459, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A solution of 700 mg of t-butyl [[1-[[1-(p-amidinobenzoyl)-2-piperidinyl]carbonyl]-4-piperidinyl]oxy]acetate in 20ml of dichloromethane and 20 ml of trfluoroacetic acid is stirred at room temperature for 3 hours and evaporated. The residue is dissolved in ethanol and treated with ether. Suction filtration and drying of the precipitate and chromatography on silica gel (RP-18, water/THF 9:1) gives 111 mg of [[1 -[[1 -(p-amidino-benzoyl)-2-piperidinyl]carbonyl]-4-piperidinyl]oxyacetic acid. M.p. 233°-234° C.

Workup

  1. customevaporated
  2. dissolutionThe residue is dissolved in ethanol
  3. additiontreated with ether
  4. filtrationSuction filtration
  5. customdrying of the precipitate and chromatography on silica gel (RP-18, water/THF 9:1)

Sources & evidence

ORD record
ord-8dc2a6845e9240feaa17678cf893d211
Source dataset
uspto-grants-1996_08
Patent number
US05545658

Reaction notes

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