Sodium Chloride → HCID 9947001, compound

HRID 1292460Notes

Reaction equation

HRID 1292460 reaction equation
[CH3:1][N:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[C:4]2[CH2:11][CH2:12][C:13]3([CH2:18][CH2:17][NH:16][CH2:15][CH2:14]3)[C:3]1=2.C(N(CC)CC)C.Cl[CH2:27][C:28]1[CH:29]=[C:30]([O:34][CH3:35])[CH:31]=[CH:32][CH:33]=1.[Cl-].[Na+]>ClCCl>[CH3:35][O:34][C:30]1[CH:29]=[C:28]([CH2:27][N:16]2[CH2:17][CH2:18][C:13]3([C:3]4[N:2]([CH3:1])[C:10]5[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=5[C:4]=4[CH2:11][CH2:12]3)[CH2:14][CH2:15]2)[CH:33]=[CH:32][CH:31]=1

Participants

6

Procedure

A solution of 1,4-dihydro-4-methylspiro[cyclopent[b]indole-3(2H),4'-piperidine] (2.5 g) and triethylamine (2.9 ml) in dichloromethane (100 ml) and 3-(chloromethyl)anisole (1.95 g) was stirred overnight at ambient temperature, under nitrogen. Saturated sodium chloride solution was added and the mixture was extracted with dichloromethane. The extracts were dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was flashed chromatographed (silica gel), eluting with 10% anhydrous acetone/dichloromethane. The appropriate fractions were collected and concentrated to give 1.3 g (35%) of product, mp 100°-101° C.

Workup

  1. extractionthe mixture was extracted with dichloromethane
  2. dry with materialThe extracts were dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated in vacuo
  5. customThe residue was flashed chromatographed (silica gel)
  6. washeluting with 10% anhydrous acetone/dichloromethane
  7. customThe appropriate fractions were collected
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-7581da67bde84a2d8913b165ea501c6d
Source dataset
uspto-grants-1998_05
Patent number
US05756743

Reaction notes

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