Hydrochloric Acid → HCID 67425135, compound

HRID 573075Notes

Reaction equation

HRID 573075 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[CH:14]([N:16]2[CH2:21][CH2:20][N:19]([C:22]3[CH:32]=[CH:31][C:25]([C:26]([O:28]CC)=[O:27])=[C:24]([O:33][C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=4[Cl:40])[CH:23]=3)[CH2:18][CH2:17]2)[CH3:15])=[CH:4][CH:3]=1.[OH-].[Na+].Cl>O1CCCC1.CO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[CH:14]([N:16]2[CH2:17][CH2:18][N:19]([C:22]3[CH:32]=[CH:31][C:25]([C:26]([OH:28])=[O:27])=[C:24]([O:33][C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=4[Cl:40])[CH:23]=3)[CH2:20][CH2:21]2)[CH3:15])=[CH:4][CH:3]=1

Participants

6

Procedure

A mixture of EXAMPLE 110D (300 mg) in tetrahydrofuran (10 mL) and methanol (10 mL) at 50° C. was treated with 10% NaOH (2085 μL), stirred overnight, neutralized with HCl and concentrated. The concentrate was taken up in water and extracted with dichloromethane. The organic layer was dried over Na2SO4, filtered and concentrated.

Workup

  1. concentrationconcentrated
  2. extractionextracted with dichloromethane
  3. dry with materialThe organic layer was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-517e2d3208d342cab61933335a57bb17
Source dataset
uspto-grants-2015_05
Patent number
US09029404B2

Reaction notes

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