2-Thiophenecarboxylic acid → Thiophene-2-carboxylic Acid [3-(4-amino-pyrazolo[3,4-d]pyrimidin-1-yl)-phenyl]-amide

HRID 655858Notes

Reaction equation

HRID 655858 reaction equation
N[C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12]3=[N:13][CH:14]=[N:15][C:16]([NH2:17])=[C:11]3[CH:10]=[N:9]2)=[CH:4][CH:3]=1.[S:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[C:23]([OH:25])=O.Cl.C[N:28](C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1>CN(C=O)C.CO>[NH2:17][C:16]1[N:15]=[CH:14][N:13]=[C:12]2[N:8]([C:5]3[CH:4]=[C:3]([NH:28][C:23]([C:19]4[S:18][CH:22]=[CH:21][CH:20]=4)=[O:25])[CH:2]=[CH:7][CH:6]=3)[N:9]=[CH:10][C:11]=12

Participants

7

Reactant 4

HCID 107002-Thiophenecarboxylic acidHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 119959601-(4-Amino-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine

Product 1

HCID 11996256Thiophene-2-carboxylic Acid [3-(4-amino-pyrazolo[3,4-d]pyrimidin-1-yl)-phenyl]-amideYield 13%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 6228DimethylformamideSolvent

Procedure

Title compound 11A, 1-(4-amino-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine (39 mg, 1.1 eq, 0.17 mmol) was added to a solution 2-thiophenecarboxylic acid (20 mg, 1.0 eq, 0.16 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (27 mg, 1.1 eq, 0.17 mmol), 1-hydroxybenzotriazole (21 mg, 1.0 eq, 0.16 mmol) in DMF (1 ml) which had been stirred for 10 minutes under an inert atmosphere. The reaction was stirred at room temperature for 17 hours, after which methanol (1 ml) was added, and the solvents were removed in vacuo. The residue was then triturated with methanol and the resultant solid was isolated by filtration to yield the title compound as a pale yellow solid (7.3 mg, 0.02 mmol, 13%). LCMS: [M+H]+=337, Rt=1.58 min, 100% purity.

Workup

  1. stirringThe reaction was stirred at room temperature for 17 hours
  2. customthe solvents were removed in vacuo
  3. customThe residue was then triturated with methanol
  4. customthe resultant solid was isolated by filtration

Sources & evidence

ORD record
ord-305f302d821648d2ab7d36c10e6298d4
Source dataset
uspto-grants-2011_12
Patent number
US08071607B2

Reaction notes

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