Hydrochloric Acid → HCID 57899137, compound

HRID 1470282Notes

Reaction equation

HRID 1470282 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-46c5f3330fee41609325616387fd6f3e
Source dataset
uspto-grants-2015_04
Patent number
US09006430B2

Reaction notes

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