ChemicalBook--->CAS DataBase List--->1146629-75-5

1146629-75-5

1146629-75-5 Structure

1146629-75-5 Structure
IdentificationBack Directory
[Name]

(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl pivalate
[CAS]

1146629-75-5
[Synonyms]

(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl pivalate
(4-Chloro-7h-pyrrolo[2,3-d]pyrimidin-7-yl)metethyl pivlateala
(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl 2,2-dimethylpropanoate
Propanoic acid, 2,2-dimethyl-, (4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl ester
[Molecular Formula]

C12H14ClN3O2
[MDL Number]

MFCD29060065
[MOL File]

1146629-75-5.mol
[Molecular Weight]

267.711
Chemical PropertiesBack Directory
[Boiling point ]

390.0±32.0 °C(Predicted)
[density ]

1.30±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

2.81±0.30(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C12H14ClN3O2/c1-12(2,3)11(17)18-7-16-5-4-8-9(13)14-6-15-10(8)16/h4-6H,7H2,1-3H3
[InChIKey]

DTPDTZKIIYSQPO-UHFFFAOYSA-N
[SMILES]

C(OCN1C2C(C=C1)=C(Cl)N=CN=2)(=O)C(C)(C)C
[CAS DataBase Reference]

1146629-75-5
Questions And AnswerBack Directory
[Uses]

(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl pivalate can be used as a heterocyclic derivative for pharmaceutical synthesis.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl pivalate(1146629-75-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Chloromethyl pivalate

18997-19-8

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine

3680-69-1

(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl pivalate

1146629-75-5

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine (25 g) and chloromethyl pivalate (27 g) were used as raw materials and potassium carbonate (27 g) and N,N-dimethylformamide (100 mL) were added to the reaction vessel. The reaction mixture was stirred at ambient temperature for 14 h. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, water (250 mL) was added to the mixture and stirring was continued for 2 hours. Subsequently, the reaction mixture was filtered, the filter cake was washed with water (50 mL) and finally dried under reduced pressure at 40 °C to 45 °C for 12 h to afford (4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl pivalate in 98.85% yield.

[References]

[1] Patent: WO2016/88094, 2016, A1. Location in patent: Page/Page column 10
[2] Organic Letters, 2009, vol. 11, # 9, p. 1999 - 2002
[3] Patent: US2010/190981, 2010, A1. Location in patent: Page/Page column 73-75
[4] Patent: CN107226814, 2017, A. Location in patent: Paragraph 0039-0040; 0042; 0044; 0046; 0048; 0050
[5] Patent: US2009/233903, 2009, A1. Location in patent: Page/Page column 67-68
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