Triethylamine → HCID 178451226, compound

HRID 390562Notes

Reaction equation

HRID 390562 reaction equation
[C:1]([O:5][C:6](=[O:19])[CH2:7][N:8]1[C:12]2=[N:13][CH:14]=[CH:15][CH:16]=[C:11]2[C:10]([C:17]#[N:18])=[N:9]1)([CH3:4])([CH3:3])[CH3:2].Cl.[NH2:21][OH:22].CCN(CC)CC>CCO>[C:1]([O:5][C:6](=[O:19])[CH2:7][N:8]1[C:12]2=[N:13][CH:14]=[CH:15][CH:16]=[C:11]2[C:10]([C:17](=[NH:18])[NH:21][OH:22])=[N:9]1)([CH3:4])([CH3:2])[CH3:3]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 443297Hydroxyamine hydrochlorideHCID 57978082(3-Cyano-pyrazolo[3,4-b]pyridin-1-yl)-acetic acid tert-butyl ester

Product 1

HCID 178451226HCID 178451226, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
65 °C

Procedure

A mixture of (3-cyano-pyrazolo[3,4-b]pyridin-1-yl)-acetic acid tert-butyl ester, hydroxylamine hydrochloride (8.28 g) and Et3N (22.6 mL) in EtOH (120 mL) was heated over night under N2 at 65° C. The mixture was cooled to room temperature, filtered and the collected solid was washed with H2O (100 mL) and Et2O (50 mL×2) to afforded [3-(N-hydroxycarbamimidoyl)-pyrazolo[3,4-b]pyridin-1-yl]-acetic acid tert-butyl ester.

Workup

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered
  3. washthe collected solid was washed with H2O (100 mL) and Et2O (50 mL×2)

Sources & evidence

ORD record
ord-a45b1956b16c47aabb611d80f3352200
Source dataset
uspto-grants-2013_02
Patent number
US08383630B2

Reaction notes

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