Ammonia → Benzyl 4-sulfamoylpiperidine-1-carboxylate

HRID 2388909Notes

Reaction equation

HRID 2388909 reaction equation
Cl[S:2]([CH:5]1[CH2:10][CH2:9][N:8]([C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:12])[CH2:7][CH2:6]1)(=[O:4])=[O:3].[NH3:21]>>[NH2:21][S:2]([CH:5]1[CH2:10][CH2:9][N:8]([C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:12])[CH2:7][CH2:6]1)(=[O:4])=[O:3]

Participants

3

Reactant 2

HCID 222AmmoniaHCID 21931260Benzyl 4-(chlorosulfonyl)piperidine-1-carboxylate

Product 1

HCID 59353042Benzyl 4-sulfamoylpiperidine-1-carboxylate

Procedure

To a solution of 0.88 NH3 (50 ml) was added benzyl 4-(chlorosulfonyl)piperidine-1-carboxylate (4 g) and the reaction stirred for 72 h at RT. The reaction was then extracted with DCM (3×150 ml). Organics were recovered, dried (MgSO4) and reduced in vacuo to give the subtitle compound as a clear oil. Yield 3.3 g

Workup

  1. extractionThe reaction was then extracted with DCM (3×150 ml)
  2. customOrganics were recovered
  3. dry with materialdried (MgSO4)

Sources & evidence

ORD record
ord-a234595c47814a00a84a277290f657a8
Source dataset
uspto-grants-2012_09
Patent number
US08269002B2

Reaction notes

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