HCID 15384053, compound → 182295-87-0
Reaction equation
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C:7]([NH:9][C@H:10]([C:16]([NH:18][C@H:19]([C:30]([OH:32])=[O:31])[CH2:20][C:21]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[NH:23][CH:22]=1)=[O:17])[CH2:11][CH2:12][C:13](=[O:15])[OH:14])=[O:8])[C@H:3]([CH2:5][CH3:6])[CH3:4]>C(O)=O>[NH2:1][C@H:2]([C:7]([NH:9][C@H:10]([C:16]([NH:18][C@H:19]([C:30]([OH:32])=[O:31])[CH2:20][C:21]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[NH:23][CH:22]=1)=[O:17])[CH2:11][CH2:12][C:13](=[O:14])[OH:15])=[O:8])[C@H:3]([CH2:5][CH3:6])[CH3:4]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 45 °C
Procedure
20.5 g Boc-Ile-Glu-Trp-Oh was dissolved in 150 ml formic acid, stirred for 3.5 h at 45° C. The solvent was evaporated under vacuum. 200 ml water was added to the residue and evaporation under vacuum was repeated. 300 ml isopropanol and 200 ml ether was added to the residue and allowed to stand for 10 h. The precipitate was then filtered and dried under vacuum. Yield: 15.3 g (75%).
Workup
- customThe solvent was evaporated under vacuum
- addition200 ml water was added to the residue and evaporation under vacuum
- addition300 ml isopropanol and 200 ml ether was added to the residue
- waitto stand for 10 h
- filtrationThe precipitate was then filtered
- customdried under vacuum
Sources & evidence
- ORD record
- ord-d381e499d7534716b5b5abedc447abef
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06159940
Reaction notes
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