Hydrochloric Acid → HCID 57899137, compound

HRID 2401561Notes

Reaction equation

HRID 2401561 reaction equation
C([O:3][C:4]([C:6]1[C:7]([N:15]2[CH2:20][CH2:19][C:18]([C:33]3[CH:38]=[CH:37][C:36]([Cl:39])=[CH:35][CH:34]=3)([CH2:21][N:22]3[C:30](=[O:31])[C:29]4[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=4)[C:23]3=[O:32])[CH2:17][CH2:16]2)=[C:8]2[CH:14]=[CH:13][NH:12][C:9]2=[N:10][CH:11]=1)=[O:5])C.Cl>[OH-].[Na+].O1CCOCC1>[Cl:39][C:36]1[CH:35]=[CH:34][C:33]([C:18]2([CH2:21][N:22]3[C:23](=[O:32])[C:24]4[C:29](=[CH:28][CH:27]=[CH:26][CH:25]=4)[C:30]3=[O:31])[CH2:17][CH2:16][N:15]([C:7]3[C:6]([C:4]([OH:5])=[O:3])=[CH:11][N:10]=[C:9]4[NH:12][CH:13]=[CH:14][C:8]=34)[CH2:20][CH2:19]2)=[CH:38][CH:37]=1

Participants

5

Procedure

4-[4-(4-Chlorophenyl)-4-(1,3-dioxo-1,3-dihydroisoindol-2-ylmethyl)-piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid ethyl ester (49 mg, 0.09 mmol) was hydrolysed in a mixture of 2M NaOH (1 mL) and 1,4-dioxane (1 mL) at 80° C. overnight. The solution was acidified by dropwise addition of conc. HCl. Solvents were evaporated and the resulting solid was filtered and washed with water, then dried. A white solid (45 mg) was obtained which was used in the next step without further purification.

Workup

  1. customSolvents were evaporated
  2. filtrationthe resulting solid was filtered
  3. washwashed with water
  4. customdried

Sources & evidence

ORD record
ord-c30d4a4066ee4ecdabda56bd91f2553f
Source dataset
uspto-grants-2014_08
Patent number
US08796293B2

Reaction notes

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