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Sulfamide → HCID 11379214, compound

HRID 455529
Notes
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Reaction equation

HRID 455529 reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[O:3][CH:2]1[CH2:10][NH2:11].[S:12](N)([NH2:15])(=[O:14])=[O:13]>O1CCOCC1>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[O:3][CH:2]1[CH2:10][NH:11][S:12]([NH2:15])(=[O:14])=[O:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 82267SulfamideHCID 573560262-(Aminomethyl)-1,3-benzodioxole

Product 1

HCID 11379214HCID 11379214, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

C-Benzo[1,3]dioxol-2-yl-methylamine (2.94 g, 19.4 mmol) and sulfamide (3.74 g, 38.9 mmol) were combined in dry dioxane (50 mL) and the solution was heated to reflux overnight. The reaction was concentrated and the residue was chromatographed (2% to 10% acetone in dichloromethane) to yield the title compound as a white solid.

Workup

  1. temperaturethe solution was heated
  2. temperatureto reflux overnight
  3. concentrationThe reaction was concentrated
  4. customthe residue was chromatographed (2% to 10% acetone in dichloromethane)

Sources & evidence

ORD record
ord-daaee8a9d99d45558e50973a824e5c29
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08497298B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes