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149765-16-2

149765-16-2 Structure

149765-16-2 Structure
IdentificationBack Directory
[Name]

Propanamide, N-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethyl-
[CAS]

149765-16-2
[Synonyms]

N2-Pivaloyl-4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyriMidine
4-chloro-5-iodo-2-pivaloylamino-7H-pyrrolo[2,3-d]pyrimidine
N-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyriMidin-2-yl)pivalaMide
Propanamide, N-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2...
N2-Pivaloyl-2-amino-?4-?chloro-?5-?iodo-?7H-?pyrrolo[2,?3-?d]?pyrimidine
N-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethylpropionamide
N-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyriMidin-2-yl)-2,2-diMethyl propanaMide
Propanamide, N-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethyl-
[Molecular Formula]

C11H12ClIN4O
[MDL Number]

MFCD11109808
[MOL File]

149765-16-2.mol
[Molecular Weight]

378.6
Chemical PropertiesBack Directory
[Melting point ]

240 °C(Solv: methanol (67-56-1))
[density ]

1.90±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

5.97±0.40(Predicted)
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P501-P270-P264-P301+P312+P330
Spectrum DetailBack Directory
[Spectrum Detail]

Propanamide, N-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethyl-(149765-16-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

N-(4-CHLORO-7H-PYRROLO[2,3-D]PYRIMIDIN-2-YL)-2,2-DIMETHYLPROPIONAMIDE

149765-15-1

Propanamide, N-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethyl-

149765-16-2

Step 4. Synthesis of N-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethylpropanamide An anhydrous tetrahydrofuran (2L) solution of N-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethylpropanamide (101 g, 0.40 mol) was treated with N-iodosuccinimide (98.9 g, 0.44 mol, 1.1 eq.) under nitrogen protection and the reaction was stirred at room temperature for 40 min. After completion of the reaction, the solvent was removed by evaporation and the residue was dissolved in dichloromethane (1.5 L) and washed sequentially with sodium sulfite solution (500 mL x 3) and saturated saline (300 mL x 3). The organic phase was dried over anhydrous sodium sulfate, concentrated, and recrystallized from methanol to give the title compound as a white powder (122 g, 81% yield, HPLC purity: 98.2%). Retention time (tR): 6.19 min. 1H-NMR (DMSO-d6) δ: 12.65 (broad single peak, 1H), 10.11 (broad single peak, 1H), 7.76 (double peak, 1H), 1.24 (single peak, 9H).

[References]

[1] Synthesis, 2004, # 8, p. 1203 - 1210
[2] Heterocycles, 1993, vol. 35, # 2, p. 825 - 841
[3] Angewandte Chemie - International Edition, 2007, vol. 46, # 13, p. 2325 - 2327
[4] Patent: US2006/223797, 2006, A1. Location in patent: Page/Page column 83-84
[5] Journal of Medicinal Chemistry, 2012, vol. 55, # 17, p. 7786 - 7795
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