Isopropyl chloroformate → HCID 57550076, compound

HRID 1676195Notes

Reaction equation

HRID 1676195 reaction equation
[CH3:1][C:2]1[C:3]([O:19][CH:20]2[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]2)=[CH:4][C:5](=[O:18])[N:6]([C:8]2[CH:13]=[CH:12][C:11]([S:14]([CH3:17])(=[O:16])=[O:15])=[CH:10][CH:9]=2)[CH:7]=1.C(N(CC)CC)C.[C:33](Cl)(=[O:38])[O:34][CH:35]([CH3:37])[CH3:36]>ClCCl>[CH3:1][C:2]1[C:3]([O:19][CH:20]2[CH2:25][CH2:24][N:23]([C:33]([O:34][CH:35]([CH3:37])[CH3:36])=[O:38])[CH2:22][CH2:21]2)=[CH:4][C:5](=[O:18])[N:6]([C:8]2[CH:13]=[CH:12][C:11]([S:14]([CH3:17])(=[O:15])=[O:16])=[CH:10][CH:9]=2)[CH:7]=1

Participants

5

Procedure

The compound obtained in Example 160, Step A (25 mg, 0.069 mmol) was dissolved in dichloromethane (0.5 mL) to which was then added triethylamine (0.029 mL, 0.207 mmol) and isopropyl carbonochloridate (10.1 mg, 0.083 mmol). After 45 minutes the solvent was removed in vacuo and the residue purified by passing through a UCT (United Chemical Technologies) 2.5 g C-18 cartridge (#CEC181(2500)6) and eluting as follows;

Workup

  1. customAfter 45 minutes the solvent was removed in vacuo
  2. customthe residue purified
  3. washeluting

Sources & evidence

ORD record
ord-6878cdc784ec40dca2a7875d3900f9f9
Source dataset
uspto-grants-2011_08
Patent number
US08003796B2

Reaction notes

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