Hydrazine hydrate (1:1) → HCID 131730606, compound

HRID 1912358Notes

Reaction equation

HRID 1912358 reaction equation
CN(C(O[N:9]1[N:18]=NC2C=CC(=CC1=2)Cl)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[NH2:26][C@H:27]([C:32]([O:34]C)=O)[CH2:28][CH:29]([CH3:31])[CH3:30].[NH:36]([C:44]([O:46]C(C)(C)C)=O)[C@H:37]([CH:42]=[O:43])[CH2:38][CH:39]([CH3:41])[CH3:40].[NH:51]([N:62]=[N+:63]=[N-:64])[C@H:52](C=O)[CH2:53][C:54]1[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=1.O.NN>CO.C1(C)C=CC=CC=1>[NH:51]([N:62]=[N+:63]=[N-:64])[C@H:52]([C:44]([NH:36][C@H:37]([C:42]([NH:26][C@H:27]([C:32]([NH:9][NH2:18])=[O:34])[CH2:28][CH:29]([CH3:30])[CH3:31])=[O:43])[CH2:38][CH:39]([CH3:40])[CH3:41])=[O:46])[CH2:53][C:54]1[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=1

Participants

8

Reactant 5

HCID 24654Hydrazine hydrate (1:1)HCID 65105(+)-L-Leucine methyl esterHCID 104275tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 42624899O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphateHCID 131730607HCID 131730607, compound

Product 1

HCID 131730606HCID 131730606, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 1140TolueneSolvent

Procedure

This compound was synthesized via general Boc-based peptide coupling procedures using HCTU from H-Leu-OMe, Boc-Leu-H and N3-Phe-H. The last step involved the introduction of the hydrazide by stirring of a mixture containing tripeptide N3-Phe-Leu-Leu-OMe (1.51 g, 3.49 mmol) and hydrazine monohydrate (30 eq., 105 mmol, 5.1 mL) in MeOH (30 mL) for 15 hours at room temperature. Compound 38 was obtained after coevaporation of the mixture with toluene (3×) as a colourless solid (yield: 1.51 g, 3.49 mmol, quant.). LC-MS: Rt (min): 6.87 (ESI-MS (m/z): 432.13 (M+H+)).

Workup

  1. customThis compound was synthesized via general Boc-

Sources & evidence

ORD record
ord-8d3d6d65d4fd4dfebc80c4078807fcd7
Source dataset
uspto-grants-2013_12
Patent number
US08609610B2

Reaction notes

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