Hydrochloric Acid → HCID 14372572, compound

HRID 1382977Notes

Reaction equation

HRID 1382977 reaction equation
[NH2:1][C:2]1[C:17]([Cl:18])=[CH:16][C:5]([C:6]([NH:8][CH2:9][CH2:10][N:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=[O:7])=[C:4]([O:19][CH2:20][CH2:21][CH2:22][S:23][CH3:24])[CH:3]=1.Cl.I([O-])(=O)(=O)=[O:27].[Na+].[OH-].[Na+]>O>[NH2:1][C:2]1[C:17]([Cl:18])=[CH:16][C:5]([C:6]([NH:8][CH2:9][CH2:10][N:11]([CH2:12][CH3:13])[CH2:14][CH3:15])=[O:7])=[C:4]([O:19][CH2:20][CH2:21][CH2:22][S:23]([CH3:24])=[O:27])[CH:3]=1

Participants

6

Procedure

To a stirred solution of product from Example 49 (1.496 g, 4 mmoles) in 2N hydrochloric acid (5.0 ml, 10 mmoles) and water (20 ml) was added sodium periodate (856 mg, 4.0 mmoles) and the mixture stirred for 2.5 hours. It was then basified with 4N sodium hydroxide (3 ml) and extracted with methylene chloride (3×30 ml). The extract was concentrated in vacuo and the residue flash-chromatographed on deactivated silica column using methylene chloride:methanol:ammonia (100:3.5:0.5) solvent system. The appropriate fractions were combined and concentrated to give a yellow oil which crystallized from methylene chloride-ether to give 770 mg of the title product as a light yellow solid, mp. 116°-117° C.

Workup

  1. extractionextracted with methylene chloride (3×30 ml)
  2. concentrationThe extract was concentrated in vacuo
  3. customthe residue flash-chromatographed on deactivated silica column
  4. concentrationconcentrated
  5. customto give a yellow oil which
  6. customcrystallized from methylene chloride-ether

Sources & evidence

ORD record
ord-207f1c5eb50e4607a867f5a6b165980e
Source dataset
uspto-grants-1989_02
Patent number
US04808624

Reaction notes

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