Hydrazine hydrate (1:1) → HCID 131713885, compound
Reaction equation
[NH:1]([C:32]([O:34][CH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)=[O:33])[C@H:2]([C:11]([NH:13][C@H:14]([C:19]([NH:21][C@H:22]([C:27](OCC)=[O:28])[CH2:23][CH:24]([CH3:26])[CH3:25])=[O:20])[CH2:15][C:16](=[O:18])[NH2:17])=[O:12])[CH2:3][C:4]1[CH:9]=[CH:8][C:7](O)=[CH:6][CH:5]=1.[OH2:42].[NH2:43][NH2:44]>CO>[NH:1]([C:32]([O:34][CH2:35][C:36]1[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=1)=[O:33])[C@H:2]([C:11]([NH:13][C@H:14]([C:19]([NH:21][C@H:22]([C:27]([NH:43][NH2:44])=[O:28])[CH2:23][CH:24]([CH3:26])[CH3:25])=[O:20])[CH2:15][C:16](=[O:18])[NH2:17])=[O:12])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:42])=[CH:6][CH:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.78 Grams of Z-Tyr-Asn-Leu-OEt was dissolved in 30 ml of methanol, further 1.21 ml of hydrazine hydrate was added to the solution and the mixture was allowed to stand overnight, the crystals formed were collected by filtration, then washed with a small amount of methanol to obtain 3.10 g of Z-Tyr-Asn-Leu-NHNH2.
Workup
- customthe crystals formed
- filtrationwere collected by filtration
- washwashed with a small amount of methanol
Sources & evidence
- ORD record
- ord-d6db2011deee46fc9c0e1c692860b975
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04474754
Reaction notes
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