Hydrochloric Acid → 956034-35-8

HRID 2403389Notes

Reaction equation

HRID 2403389 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][N:11]([S:14]([CH3:17])(=[O:16])=[O:15])[C@@H:10]([CH3:18])[CH2:9]1)=O)(C)(C)C.[ClH:19]>ClCCl.C(OCC)C>[ClH:19].[CH3:17][S:14]([N:11]1[CH2:12][CH2:13][NH:8][CH2:9][C@@H:10]1[CH3:18])(=[O:15])=[O:16]

Participants

5

Reactant 2

HCID 313Hydrochloric AcidHCID 66617785HCID 66617785, compound

Product 1

HCID 66617740956034-35-8Yield 82%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 6344DichloromethaneSolvent

Procedure

To a solution of (S)-4-methanesulfonyl-3-methyl-piperazine-1-carboxylic acid tert-butyl ester (924 mg) in dichloromethane (20 mL) at 0° C. was added dropwise HCl (6.65 mL of a 2 M solution in diethyl ether). The reaction mixture was stirred at room temperature for 2 h. The precipitate formed was then collected by filtration and dried to afford (S)-1-methanesulfonyl-2-methyl-piperazine hydrochloride salt as a white solid (583 mg, 82%).

Workup

  1. customThe precipitate formed
  2. filtrationwas then collected by filtration
  3. customdried

Sources & evidence

ORD record
ord-89f5caeab53744fb9d19dad9277920be
Source dataset
uspto-grants-2014_08
Patent number
US08802670B2

Reaction notes

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