Dichloromethane → HCID 87630457, compound

HRID 2199728Notes

Reaction equation

HRID 2199728 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([C:14]=1[CH2:15][CH2:16][CH2:17][OH:18])=[CH:12][CH:11]=[CH:10][C:9]=2[C:19]1[CH:24]=[CH:23][C:22]([C:25]([O:27][CH3:28])=[O:26])=[CH:21][C:20]=1[CH3:29])=[O:5])[CH3:2].[C:30]1(C)[C:31]([S:36](Cl)(=[O:38])=[O:37])=[CH:32][CH:33]=[CH:34][CH:35]=1.Cl[CH2:42]Cl>CN(C1C=CN=CC=1)C.C(OCC)(=O)C>[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([C:14]=1[CH2:15][CH2:16][CH2:17][O:18][S:36]([C:31]1[CH:30]=[CH:35][C:34]([CH3:42])=[CH:33][CH:32]=1)(=[O:37])=[O:38])=[CH:12][CH:11]=[CH:10][C:9]=2[C:19]1[CH:24]=[CH:23][C:22]([C:25]([O:27][CH3:28])=[O:26])=[CH:21][C:20]=1[CH3:29])=[O:5])[CH3:2]

Participants

6

Procedure

To a mixture of EXAMPLE 127B (2.0 g), toluene-2-sulfonyl chloride (1.16 g) in dichloromethane (30 mL) was added DMAP (0.305 g). The mixture was stirred at room temperature overnight. The mixture was diluted with ethyl acetate (300 mL) and washed with saturated aqueous sodium bicarbonate mixture, 3% aqueous HCl, water and brine. After drying over Na2SO4 and filtering, the mixture was concentrated.

Workup

  1. washwashed with saturated aqueous sodium bicarbonate mixture, 3% aqueous HCl, water and brine
  2. dry with materialAfter drying over Na2SO4
  3. filtrationfiltering
  4. concentrationthe mixture was concentrated

Sources & evidence

ORD record
ord-aac5ee4d6c104f59aa41ebe01b810cce
Source dataset
uspto-grants-2016_06
Patent number
US09359296B2

Reaction notes

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