天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

Home Cart 0 Sign in  

[ CAS No. 1062174-44-0 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1062174-44-0
Chemical Structure| 1062174-44-0
Structure of 1062174-44-0 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 1062174-44-0 ]

Related Doc. of [ 1062174-44-0 ]

Alternatived Products of [ 1062174-44-0 ]
Product Citations

Product Details of [ 1062174-44-0 ]

CAS No. :1062174-44-0 MDL No. :MFCD16995801
Formula : C14H20BNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ZYOHYGQNRQMVMG-UHFFFAOYSA-N
M.W : 245.13 Pubchem ID :56776842
Synonyms :

Safety of [ 1062174-44-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1062174-44-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 1062174-44-0 ]

[ 1062174-44-0 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 837392-67-3 ]
  • [ 1062174-44-0 ]
YieldReaction ConditionsOperation in experiment
87%
Stage #1: With trifluoroacetic acid In dichloromethane at 20℃; for 2 h;
Ste 3: 5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)indolineTo the solution of tert-butyl 5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)indoline-l-carboxylate (120 mg, 0.35 mmol) in CH2CI2 (5 mL) was added 2,2,2-trifluoroacetic acid (1 mL) and the resulting mixture was stirred at room temperature for 2 hours. The mixture was neutralized to pH = 8 with saturated aqueous NaHC03 and extracted with CH2CI2. The combined extracts were washed with brine, dried and concentrated in vacuo to afford the desired product (74 mg, 87percent).1H NMR (CDC13): δ 7.56 (1H, s), 7.50 (1H, d, / = 8.0 Hz), 6.60 (1H, d, / = 8.0 Hz), 3.57 (2H, t, / = 8.8 Hz), 3.02 (2H, t, / = 8.8 Hz), 1.32 (12H, s).
Reference: [1] Patent: WO2012/103806, 2012, A1, . Location in patent: Page/Page column 48
  • 2
  • [ 22190-33-6 ]
  • [ 73183-34-3 ]
  • [ 1062174-44-0 ]
YieldReaction ConditionsOperation in experiment
28% With potassium acetate In dichloromethane; dimethyl sulfoxide at 80℃; Example 46; 6-(2,3-Dihydro-1H-indol-5-yl)-4-morpholin-4-yl-1-(1-pyridin-3-ylmethyl-piperidin-4-yl)-1H-pyrazolo[3,4-d]pyrimidine (Scheme 36)1 mmol (198 mg) 5-bromoindoline, 1.5 mmol (381 mg) bispinacolatodiboron, 0.1 mmol (73 mg) Pd(dppf)Cl2.CH2Cl2 and 3 mmol (296 mg) KOAc are suspended in DMSO and heated at 80 C overnight. The mixture is diluted with EtOAc, filtered over Celite and concentrated. Flash chromatography (5-20percent EtOAc in hexanes) gave 69 mg (28percent) of the boronate. This was added to a solution of 50 mg 6-Chloro-4-morpholin-4-yl-1-(1-pyridin-3-ylmethyl-piperidin-4-yl)-1H-pyrazolo[3,4-d]pyrimidine in 2 mL DME and 250 uL of a 2M Na2CO3 solution. 10 mol percent Pd(PP3)4 was added and the mixture was stirred at 95C overnight. The solvents were removed and the product was purified by HPLC (TFA buffers).
Reference: [1] Patent: US2008/234262, 2008, A1, . Location in patent: Page/Page column 90
  • 3
  • [ 22190-33-6 ]
  • [ 1062174-44-0 ]
Reference: [1] Patent: WO2012/103806, 2012, A1,
  • 4
  • [ 261732-38-1 ]
  • [ 1062174-44-0 ]
Reference: [1] Patent: WO2012/103806, 2012, A1,
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 1062174-44-0 ]

Organoboron

Chemical Structure| 448955-87-1

[ 448955-87-1 ]

9-(2-Ethylhexyl)-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole

Similarity: 0.91

Chemical Structure| 269410-24-4

[ 269410-24-4 ]

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

Similarity: 0.88

Chemical Structure| 1219741-53-3

[ 1219741-53-3 ]

1-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

Similarity: 0.87

Chemical Structure| 642494-36-8

[ 642494-36-8 ]

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

Similarity: 0.86

Chemical Structure| 1220696-38-7

[ 1220696-38-7 ]

1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-2-one

Similarity: 0.85

Related Parent Nucleus of
[ 1062174-44-0 ]

Indolines

Chemical Structure| 1220696-38-7

[ 1220696-38-7 ]

1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-2-one

Similarity: 0.85

Chemical Structure| 893441-85-5

[ 893441-85-5 ]

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-2-one

Similarity: 0.85

Chemical Structure| 1235451-62-3

[ 1235451-62-3 ]

tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline-1-carboxylate

Similarity: 0.75

Chemical Structure| 376584-62-2

[ 376584-62-2 ]

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-one

Similarity: 0.72

Chemical Structure| 1004294-80-7

[ 1004294-80-7 ]

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-one

Similarity: 0.72

; ;