21950-36-7

  • Product Name:Adenosine, 5'-aMino-5'-deoxy-2',3'-O-(1-Methylethylidene)-
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Product Details

Purity:99%

High Quality 21950-36-7 In Stock, Adenosine, 5'-aMino-5'-deoxy-2',3'-O-(1-Methylethylidene)-

  • Molecular Formula:C13H18N6O3
  • Molecular Weight:306.324
  • Melting Point:202-203℃ 
  • Boiling Point:553.1±60.0 °C(Predicted) 
  • PKA:9.08±0.29(Predicted) 
  • PSA:123.33000 
  • Density:1.80±0.1 g/cm3 (20 oC 760 Torr) 
  • LogP:1.06620 

21950-36-7 Relevant articles

Methionyl adenylate analogues as inhibitors of methionyl-tRNA synthetase

Lee, Jeewoo,Sang, Uk Kang,Mee, Kyoung Kang,Moon, Woo Chun,Yeong, Joon Jo,Jin, Hwan Kwak,Kim, Sunghoon

, p. 1365 - 1370 (1999)

Four stable analogues of methionyl adeny...

Construction of a library of structurally diverse ribonucleopeptides with catalytic groups

Tamura, Tomoki,Nakano, Shun,Nakata, Eiji,Morii, Takashi

, p. 1 - 7 (2017)

Functional screening of structurally div...

Synthesis and evaluation of adenosine containing 3-arylfuran-2(5H)-ones as tyrosyl-tRNA synthetase inhibitors

Wei, Wei,Liu, Qi,Li, Zhen-Zhen,Shi, Wei-Kang,Fu, Xing,Liu, Jia,Zhu, Xuan,Wang, Xiao-Cong,Xu, Ning,Li, Teng-Fei,Jiang, Fu-Rui,Xiao, Zhu-Ping,Zhu, Hai-Liang

, p. 62 - 68 (2017)

Tyrosyl-tRNA synthetase (TyrRS) is an am...

Cycloalkane analogues of sinefungin as EHMT1/2 inhibitors

Liu, Qing,Cai, Xiaoqing,Yang, Dehua,Chen, Yi,Wang, Yafang,Shao, Liming,Wang, Ming-Wei

, p. 4579 - 4594 (2017)

A series of cycloalkyl substituted analo...

Purine derivative and preparation method and application thereof

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Paragraph 0166; 0211; 0216-0217, (2021/06/26)

The invention discloses a purine derivat...

Potent SARS-CoV-2 mRNA Cap Methyltransferase Inhibitors by Bioisosteric Replacement of Methionine in SAM Cosubstrate

Bobi?eva, Olga,Bobrovs, Raitis,Ka?epe, Iveta,Patetko, Liene,Kalni??, Gints,?i?ovs, Mihails,Bula, Anna L.,Grī Nberga, Solveiga,Borodu??is, Mā Rti??,Ramata-Stunda, Anna,Rostoks, Nils,Jirgensons, Aigars,Tā Rs, Kaspars,Jaudzems, Kristaps

supporting information, p. 1102 - 1107 (2021/06/30)

Viral mRNA cap methyltransferases (MTase...

BROAD SPECTRUM ANTI-CANCER COMPOUNDS

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Page/Page column 375-376, (2021/04/23)

Described herein, inter alia, are compou...

Chemo-selective Rh-catalysed hydrogenation of azides into amines

Galan, M. Carmen,Ghirardello, Mattia,Ledru, Helene,Sau, Abhijit

supporting information, (2020/02/18)

Rh/Al2O3 can be used as an effective che...

21950-36-7 Process route

5'-azido-5'-deoxy-2',3'-O-isopropylidene adenosine
34245-48-2

5'-azido-5'-deoxy-2',3'-O-isopropylidene adenosine

5'-amino-5'-deoxy-2',3'-O-isopropylideneadenosine
21950-36-7

5'-amino-5'-deoxy-2',3'-O-isopropylideneadenosine

Conditions
Conditions Yield
With palladium 10% on activated carbon; hydrogen; In methanol;
100%
With palladium on activated charcoal; hydrogen; In ethanol;
100%
With hydrazine hydrate; In ethanol; at 20 ℃; chemoselective reaction;
98%
With palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 16h;
95%
With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃; for 5h;
90%
With palladium on activated charcoal; hydrogen; In methanol; at 20 ℃; for 2.5h;
88%
With triphenylphosphine; In pyridine; ammonium hydroxide; at 20 ℃;
84%
With hydrogen; palladium on activated charcoal; In ethanol; for 5h; under 2327.2 Torr;
70%
5'-azido-5'-deoxy-2',3'-O-isopropylidene adenosine; In tetrahydrofuran; at 20 ℃; for 4h; Inert atmosphere;
With water; In tetrahydrofuran; at 20 ℃; Inert atmosphere;
70%
With palladium 10% on activated carbon; hydrogen; In ethanol; for 12h; under 760.051 Torr;
68%
With Rh/Al2O3; hydrogen; acetic acid; In ethyl acetate; toluene; at 20 ℃; for 24h; under 760.051 Torr; chemoselective reaction;
65%
With ammonium hydroxide; triphenylphosphine; In pyridine; for 18h; Yield given; Ambient temperature;
 
Multi-step reaction with 2 steps
1: tetrahydrofuran / 1 h / 20 °C
2: H2O / 60 °C
With water; In tetrahydrofuran; 1: Staudinger reaction;
 
With palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 18h;
2.21 g
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 4h;
 
With 5%-palladium/activated carbon; hydrogen;
 
With palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 20 ℃; for 3h;
850 mg
With palladium on activated charcoal; hydrogen; In methanol; for 4h;
 
2-[[(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]methyl]-2,3-dihydro-1H-isoindol-1,3-dione
80860-44-2

2-[[(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]methyl]-2,3-dihydro-1H-isoindol-1,3-dione

5'-amino-5'-deoxy-2',3'-O-isopropylideneadenosine
21950-36-7

5'-amino-5'-deoxy-2',3'-O-isopropylideneadenosine

Conditions
Conditions Yield
With hydrazine hydrate; In ethanol; for 2h; Heating;
96%
With ethanol; hydrazine hydrate; at 80 ℃; for 2h;
96.4%
With hydrazine hydrate; In ethanol;
93%
With hydrazine hydrate; In ethanol; Reflux;
90.5%
With hydrazine hydrate; In ethanol; Reflux;
78%
With hydrazine; In ethanol;
78%
With methylhydrazine; In ethanol; at 15 - 40 ℃; for 18h;
78%
With hydrazine hydrate; In ethanol; Heating;
77%
With hydrazine hydrate; In ethanol; at 20 ℃; for 3h; Reflux;
76%
With hydrazine hydrate; In ethanol; for 2h; Reflux;
64%
With hydrazine hydrate; In ethanol; Reflux;
 
With hydrazine hydrate; In ethanol; at 80 ℃; for 1.5h;
 
With hydrazine hydrate; In ethanol; at 80 ℃; for 1.5h;
 
With hydrazine hydrate; In ethanol; Reflux;
 
With hydrazine hydrate; In ethanol; at 85 ℃; for 2h;
 
With hydrazine hydrate; In ethanol; at 80 ℃; for 2h;
 

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    2-[[(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]methyl]-2,3-dihydro-1H-isoindol-1,3-dione

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    5'-azido-5'-deoxy-2',3'-O-isopropylidene adenosine

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    ((3aR,4R,6R,6aR)-6-(6-benzamido-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl 4-methylbenzenesulfonate

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    2,3,4,5,6-pentafluorophenol

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    (1S,5R,7S)-1,5,7-Trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-{[(3aR,4R,6R,6aR)-6-(6-amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl]-carbamoyl}-naphthalen-2-yl ester

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    124650-88-0

    1,5,7-Trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-{[(3aS,4S,6S,6aS)-6-(6-amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl]-carbamoyl}-naphthalen-2-yl ester