Hydrochloric Acid → HCID 7023251, compound

HRID 2273723Notes

Reaction equation

HRID 2273723 reaction equation
[NH2:1][C@H:2]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[CH2:3][C:4]([OH:6])=[O:5].[CH2:12]([O:19][C:20](Cl)=[O:21])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.O1CCOCC1.Cl>[OH-].[Na+]>[CH2:12]([O:19][C:20]([NH:1][C@H:2]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[CH2:3][C:4]([OH:6])=[O:5])=[O:21])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 10387Benzyl chloroformateHCID 312751,4-DioxaneHCID 86716(S)-3-Amino-3-(thiophen-2-yl)propanoic acid

Product 1

HCID 7023251HCID 7023251, compound

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

(S)-3-amino-3-(thiophen-2-yl)propanoic acid (0.894 g) and benzyloxycarbonyl chloride 0.980 g) were stirred in 2M NaOH (8 mL) and dioxane (26 mL) at 0° C. for 24 hours. The reaction mixture was acidified with concentrated aqueous HCl, extracted twice with ethyl acetate, and the extracts were dried over MgSO4, filtered, concentrated, and chromatographed on silica gel with 50% ethyl acetate/hexanes.

Workup

  1. extractionextracted twice with ethyl acetate
  2. dry with materialthe extracts were dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customchromatographed on silica gel with 50% ethyl acetate/hexanes

Sources & evidence

ORD record
ord-f31a32a6c215443699c1c87b2e3d843a
Source dataset
uspto-grants-2015_09
Patent number
US09125913B2

Reaction notes

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