HCID 19757885, compound → HCID 19757919, compound
Reaction equation
C(OC([N:8]([S:60]([C:63]1[CH:68]=[CH:67][C:66]([CH3:69])=[CH:65][CH:64]=1)(=[O:62])=[O:61])[CH2:9][CH2:10][CH2:11][CH2:12][N:13]([C:52](=[O:59])[C:53]1[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][N:21]([C:44](=[O:51])[C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1)[CH2:22][CH2:23][CH2:24][CH2:25][N:26](C(OC(C)(C)C)=O)[S:27]([C:30]1[CH:35]=[CH:34][C:33]([CH3:36])=[CH:32][CH:31]=1)(=[O:29])=[O:28])=O)(C)(C)C>Cl>[CH3:36][C:33]1[CH:32]=[CH:31][C:30]([S:27]([NH:26][CH2:25][CH2:24][CH2:23][CH2:22][N:21]([C:44](=[O:51])[C:45]2[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=2)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][N:13]([C:52](=[O:59])[C:53]2[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=2)[CH2:12][CH2:11][CH2:10][CH2:9][NH:8][S:60]([C:63]2[CH:64]=[CH:65][C:66]([CH3:69])=[CH:67][CH:68]=2)(=[O:62])=[O:61])(=[O:28])=[O:29])=[CH:35][CH:34]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolve 1,19-Bis(tert-butyloxycarbonyl)-1,19-bis[(4-methylphenyl)sulfonyl]-6,14-bis(benzoyl)-1,6,14,19-tetraazanonadecane (9.76 g, 10 mmol) in saturated methanolic hydrochloric acid (100 mL). Stir for several hours and evaporate the solvent in vacuo. Dissolve the residue in water and neutralize with saturated sodium hydrogen carbonate and extract with ethyl acetate. Dry (MgSO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography to give the title compound.
Workup
- customevaporate the solvent in vacuo
- dissolutionDissolve the residue in water
- extractionextract with ethyl acetate
- dry with materialDry (MgSO4)
- customevaporate the solvent in vacuo
- customPurify by silica gel chromatography
Sources & evidence
- ORD record
- ord-51273a50ac7b47d580626bcfb359b914
- Source dataset
- uspto-grants-1993_06
- Patent number
- US05217964
Reaction notes
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