Hydrochloric Acid → HCID 178427600, compound

HRID 636674Notes

Reaction equation

HRID 636674 reaction equation
[S:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[Li]CCCC.[NH:11]([C:36]([O:38][C:39]([CH3:42])([CH3:41])[CH3:40])=[O:37])[C@H:12]([C:30](N(OC)C)=[O:31])[CH2:13][CH2:14][CH2:15][NH:16][C:17](=[NH:29])[NH:18][S:19]([C:22]1[CH:28]=[CH:27][C:25]([CH3:26])=[CH:24][CH:23]=1)(=[O:21])=[O:20].[Li]C1SC=CN=1.Cl.C1C[O:53]CC1>>[NH:11]([C:36]([O:38][C:39]([CH3:42])([CH3:40])[CH3:41])=[O:37])[C@H:12]([C:30]([OH:53])=[O:31])[CH2:13][CH2:14][CH2:15][NH:16][C:17](=[NH:29])[NH:18][S:19]([C:22]1[CH:28]=[CH:27][C:25]([CH3:26])=[CH:24][CH:23]=1)(=[O:20])=[O:21].[S:1]1[CH:5]=[CH:4][N:3]=[CH:2]1

Participants

7

Reactant 6

HCID 313Hydrochloric AcidHCID 8028Tetrahydrofuran2×HCID 9256ThiazoleHCID 178418339ButyllithiumHCID 178502742HCID 178502742, compoundHCID 178506781HCID 178506781, compound

Product 1

HCID 178427600HCID 178427600, compoundYield 84%

Procedure

To a solution of thiazole (2.5 g, 29 mmol) in THF (25 mL) at −78° C. is added n-BuLi (1.6 M in hexane, 19 mL) dropwise. The mixture is stirred for 30 min. Then a solution of Boc-Arg(Tos)-N(Me)OMe (1.7 g, 3.6 mmol) in THF (50 mL) is added to the lithiothiazole mixture at −78° C. The solution is stirred for 2 h. 1M HCl (30 mL) is added to the reaction mixture and warmed to room temperature. The mixture is extracted with EtOAc (100 mL). The organic layer is washed with sat. NaCl (30 mL), dried over MgSO4, filtered and evaporated. The crude oily residue is purified by flash column over SiO2 (50% EtOAc in CH2Cl2) to give Boc-Arg(Tos)-Thiazole (1.5 g, 84% yield) as a powder. DCI -MS (M+H)+=496

Workup

  1. stirringThe solution is stirred for 2 h
  2. extractionThe mixture is extracted with EtOAc (100 mL)
  3. washThe organic layer is washed with sat. NaCl (30 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude oily residue is purified by flash column over SiO2 (50% EtOAc in CH2Cl2)

Sources & evidence

ORD record
ord-6afac08ad4ae4e44a3c8a600244f55f8
Source dataset
uspto-grants-2001_02
Patent number
US06194435B1

Reaction notes

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