Dimethylamine → ((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-carbamic acid tert-butyl ester

HRID 1879460Notes

Reaction equation

HRID 1879460 reaction equation
[CH3:1][NH:2][CH3:3].[C:4]([O:8][C:9]([NH:11][C@@H:12]([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])[CH2:13]OS(C1C=CC(C)=CC=1)(=O)=O)=[O:10])([CH3:7])([CH3:6])[CH3:5]>N1C=CC=CC=1.[OH-].[K+]>[C:4]([O:8][C:9](=[O:10])[NH:11][C@H:12]([CH2:13][N:2]([CH3:3])[CH3:1])[CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:7])([CH3:6])[CH3:5]

Participants

5

Procedure

Dimethylamine (11.2 g, 249.3 mmol, 30.0 equiv) was added portionwise to a stirred solution of toluene-4-sulfonic acid(S)-2-tert-butoxycarbonylamino-4,4-dimethyl-pentyl ester (3.2 g, 8.31 mmol, 1.0 equiv.) in pyridine (9.6 mL) at 0° C. The reaction mixture was slowly warmed to room temperature and stirred for an additional 20 hours at the same temperature. The reaction mixture was diluted with the addition of an aqueous solution of 10% potassium hydroxide (w/v; 30 mL) and was extracted with dichloromethane (3×150 mL). The collected organic extracts were dried over anhydrous sodium sulfate, concentrated under reduced pressure to obtain a crude mass. This was purified by purified by silica gel column chromatography (100-200 mesh) using a gradient of 2-5% methanol/dichloromethane to give ((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-carbamic acid tert-butyl ester (1.4 g, 65%).

Workup

  1. extractionwas extracted with dichloromethane (3×150 mL)
  2. dry with materialThe collected organic extracts were dried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customto obtain a crude mass
  5. customThis was purified
  6. customby purified by silica gel column chromatography (100-200 mesh)

Sources & evidence

ORD record
ord-3b116bd77e954d97ae2d9c88fd99ca7d
Source dataset
uspto-grants-2012_11
Patent number
US08314250B2

Reaction notes

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