1985607-70-2

(R)-7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione

(R)-7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione

别名:
CasNo.: 1985607-70-2
分子式:
分子量: 327.34
储存条件:
在线咨询
中文名称: (R)-7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione
英文名称: (R)-7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione
CasNo.: 1985607-70-2
分子式:
分子量: 327.34

Chinese Manufacturer Supply (R)-7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione 1985607-70-2 On Stock with Competitive Price

  • Molecular Formula:C17H17N3O4
  • Molecular Weight:327.34
  • Boiling Point:575.3±60.0 °C(Predicted) 
  • Density:1.43±0.1 g/cm3(Predicted) 

1985607-70-2 Relevant articles

Synthesis method of baloxavir marboxil intermediate polycyclic carbamoyl pyridone

-

Paragraph 0022-0030, (2021/05/12)

The invention provides a synthesis metho...

A series of new polycyclic carbamoyl pyridone analogues were synthesized by using chloroacetaldehyde as a substrate

Hu, Xueyuan,Kuang, Qiulin,Li, Dan,Wang, Qiang,Wu, Huili,Yuan, Jianyong

supporting information, (2021/06/02)

A facile, universal and economical metho...

Preparation method of fused ring pyridone compound

-

Paragraph 0073-0078; 0079-0082; 0083-0086; 0087-0090, (2021/04/28)

The invention relates to a preparation m...

Preparation method of balosavir intermediate

-

, (2021/01/28)

The invention relates to a preparation m...

1985607-70-2 Process route

allyl 3-((3-(benzyloxy)-2-(ethoxycarbonyl)-4-oxopyridin-1(4H)-yl)amino)morpholine -4-formate

allyl 3-((3-(benzyloxy)-2-(ethoxycarbonyl)-4-oxopyridin-1(4H)-yl)amino)morpholine -4-formate

7-(benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido [2,1-f][1,2,4]triazine-6,8-diketone
1985607-70-2,1370250-39-7

7-(benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido [2,1-f][1,2,4]triazine-6,8-diketone

Conditions
Conditions Yield
With morpholine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; at 20 ℃; for 2h;
100%
With morpholine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; at 20 ℃; for 2h;
100%
With morpholine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; for 3h; Inert atmosphere;
90%
With morpholine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; at 20 ℃; for 2h;
 
With morpholine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; at 20 ℃; for 2h;
418 mg
With morpholine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; at 20 ℃; for 2.5h;
 
With morpholine; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; at 20 ℃; for 2h;
418 mg
C<sub>22</sub>H<sub>23</sub>N<sub>3</sub>O<sub>6</sub>

C22H23N3O6

(R)-7-(benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]pyrano[4,3-c]pyrido[2,1-f][1,2,4]triazine-6,8(1H,3H)-dione
1985607-70-2,1370250-39-7

(R)-7-(benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]pyrano[4,3-c]pyrido[2,1-f][1,2,4]triazine-6,8(1H,3H)-dione

Conditions
Conditions Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 30 ℃; for 0.5h;
93.46%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 20 ℃; for 0.666667h;
91%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 20 ℃; for 0.5h;
90%
C22H23N3O6; With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 20 ℃; for 0.5h;
In di-isopropyl ether; at 20 ℃; for 0.5h;
89.9%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 20 ℃; for 0.5h;
89.9%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 20 ℃; for 0.5h;
89.9%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethanol; at 20 ℃; for 0.5h;
89.9%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; ethyl acetate; at 20 - 30 ℃; for 1h;
45%

1985607-70-2 Upstream products

  • 1332855-94-3
    1332855-94-3

    3-(benzyloxy)-4-oxo-4H-pyran-2-carboxylate ethyl ester

  • 1985607-66-6
    1985607-66-6

    1‐amino‐3‐(benzyloxy)‐4‐oxo-1,4-dihydropyridine‐2‐carboxylic acid ethyl ester

  • 119736-16-2
    119736-16-2

    3-(benzyloxy)-1-((tert-butoxycarbonyl)amino)-4-oxo-1,4-dihydropyridine-2-carboxylic acid ethyl ester

  • 2136287-59-5
    2136287-59-5

    methyl 1-((tert-butoxycarbonyl)amino)-3-(benzyloxy)-4-oxo-1,4-dihydropyridine-2-carboxylic acid

1985607-70-2 Downstream products

  • 1985605-59-1
    1985605-59-1

    (R)-12-((S)-7,8-difluoro-6,11-dihydrodibenzo[b,e]thiepin-11-yl)-7-hydroxy-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione

暂无数据
暂无数据