Hydrochloric Acid → HCID 135841608, compound

HRID 375382Notes

Reaction equation

HRID 375382 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:25]=[CH:26][C:27]=1[O:28]COC)/[CH:6]=[CH:7]/[C:8]1[NH:16][C:15]2[C:14](=[O:17])[N:13]([CH2:18][CH2:19][CH3:20])[C:12](=[O:21])[N:11]([CH2:22][CH2:23][CH3:24])[C:10]=2[N:9]=1.Cl.[OH-].[Na+].O>O1CCCC1>[OH:28][C:27]1[CH:26]=[CH:25][C:5](/[CH:6]=[CH:7]/[C:8]2[NH:16][C:15]3[C:14](=[O:17])[N:13]([CH2:18][CH2:19][CH3:20])[C:12](=[O:21])[N:11]([CH2:22][CH2:23][CH3:24])[C:10]=3[N:9]=2)=[CH:4][C:3]=1[O:2][CH3:1]

Participants

6

Procedure

Compound 194 (1.00 g, 2.33 mmol) obtained in Reference Example 133 was dissolved in 10 ml of tetrahydrofuran. To the solution was added 6 ml of 2N hydrochloric acid, and the mixture was heated under reflux for one hour. The reaction solution was neutralized with a 2N aqueous solution of sodium hydroxide under ice cooling. Water was added thereto, and the deposited crystals were collected by filtration. The obtained crude crystals were recrystallized from methanol/water to give 291 mg (yield 32%) of Compound 196 as a yellow powder.

Workup

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for one hour
  3. filtrationthe deposited crystals were collected by filtration
  4. customThe obtained crude crystals
  5. customwere recrystallized from methanol/water

Sources & evidence

ORD record
ord-4f95922336c243b29c29131738b0d39f
Source dataset
uspto-grants-1996_01
Patent number
US05484920

Reaction notes

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