Benzylamine → HCID 178522804, compound

HRID 1843615Notes

Reaction equation

HRID 1843615 reaction equation
Cl.C(N=C=NCCCN(C)C)C.ON1C2C=CC=CC=2N=N1.CCN(C(C)C)C(C)C.Cl.[N:33]1[CH:38]=[CH:37][C:36]([C:39]2[C:40]([C:44]3[CH:45]=[C:46]([CH:50]=[CH:51][CH:52]=3)[C:47]([OH:49])=O)=[N:41][NH:42][CH:43]=2)=[CH:35][CH:34]=1.[CH2:53]([NH2:60])[C:54]1[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=1>C(Cl)Cl.CN(C=O)C.O>[CH2:53]([NH:60][C:47](=[O:49])[C:46]1[CH:50]=[CH:51][CH:52]=[C:44]([C:40]2[C:39]([C:36]3[CH:35]=[CH:34][N:33]=[CH:38][CH:37]=3)=[CH:43][NH:42][N:41]=2)[CH:45]=1)[C:54]1[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=1

Participants

9

Procedure

A solution of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (0.029 g, 0.15 mmol, 1.5 eq) in dry DCM (1 mL) and a solution of 1-hydroxybenzotriazole (0.020 g, 0.15 mmol, 1.5 eq) and DIPEA (0.064 g, 0.50 mmol, 5 eq) in dry DMF (0.1 mL) were added to 3-(4-pyridin-4-yl-1H-pyrazol-3-yl)-benzoic acid hydrochloride (0.030 g, 0.10 mmol, 1 eq) in dry DMF (0.200 ml). Benzylamine (2 eq) was added to the reaction mixture, which was stirred at room temperature for 24 h. Distilled water (1.5 mL) was poured into the suspension that was stirred for 1 h at room temperature and the organic layer was separated by filtration through Alltech Separator Tube. The solvent was evaporated and reverse phase purification of the crude afforded the final product as a solid.

Workup

  1. stirringwas stirred for 1 h at room temperature
  2. customthe organic layer was separated by filtration through Alltech Separator Tube
  3. customThe solvent was evaporated
  4. customreverse phase purification of the crude

Sources & evidence

ORD record
ord-cb49706e37cd4672a979e9684bdc5f34
Source dataset
uspto-grants-2015_02
Patent number
US08946250B2

Reaction notes

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