Potassium Carbonate → 1-(tert-butylsulfinylamino)-N'-hydroxycyclobutane-1-carboximidamide

HRID 1854743Notes

Reaction equation

HRID 1854743 reaction equation
C(=O)([O-])[O-].[K+].[K+].Cl.[NH2:8][OH:9].[C:10]([C:12]1([NH:16][S:17]([C:19]([CH3:22])([CH3:21])[CH3:20])=[O:18])[CH2:15][CH2:14][CH2:13]1)#[N:11]>CCO>[CH3:20][C:19]([CH3:22])([S:17]([NH:16][C:12]1(/[C:10](=[N:8]/[OH:9])/[NH2:11])[CH2:13][CH2:14][CH2:15]1)=[O:18])[CH3:21]

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 90402316HCID 90402316, compound

Product 1

HCID 904023191-(tert-butylsulfinylamino)-N'-hydroxycyclobutane-1-carboximidamideYield 52.4%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
60 °C

Procedure

Potassium carbonate (1.38 g, 9.98 mmol) was added to a stirring solution of hydroxylamine hydrochloride (347 mg, 4.99 mmol) and N-(1-cyanocyclobutyl)-2-methylpropane-2-sulfinamide (500 mg, 2.50 mmol) in EtOH (8 ml) at rt. The reaction was then heated to 60° C. for 16 h. The mixture was then concentrated and the resulting residue was diluted with EtOAc and washed with H2O followed by sat NaCl (aq). The organic phase was dried over Na2SO4, filtered and concentrated to give the expected product (Z)-1-(1,1-dimethylethylsulfinamido)-N′-hydroxycyclobutanecarboximidamide (305 mg, 1.31 mmol, 52% yield) as a white solid consistent by LCMS and NMR. LC-MS retention time: 0.456 min; m/z (MH+): 234. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Phenomenex-Luna 3u C18 2.0×30 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 1 mL/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 2 min, a hold time of 1 min, and an analysis time of 3 min where solvent A was 10% acetonitrile/90% H2O/0.1% trifluoroacetic acid and solvent B was 10% H2O/90% acetonitrile/0.1% trifluoroacetic acid. MS data was determined using a Micromass Platform for LC in electrospray mode. 1H NMR (400 MHz, DMSO-d6) δ 9.20 (s, 1H), 5.60 (s, 1H), 5.10 (s, 2H), 2.35-2.30 (m, 1H), 2.27-2.17 (m, 1H), 2.10-2.03 (m, 1H), 1.99 (s, 1H), 1.80-1.75 (m, 1H), 1.73-1.62 (m, 1H), 1.13 (s, 9H).

Workup

  1. concentrationThe mixture was then concentrated
  2. additionthe resulting residue was diluted with EtOAc
  3. washwashed with H2O
  4. dry with materialThe organic phase was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-256b2c7cdcf14348ae24be632d1557d2
Source dataset
uspto-grants-2015_02
Patent number
US08962651B2

Reaction notes

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