3-(4-Phenoxy-phenyl)-1-piperidin-3-y-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine
- CAS:1022150-12-4
- purity:99%
Details
Top Quality Chinese Manufacturer supply 1022150-12-4 3-(4-Phenoxy-phenyl)-1-piperidin-3-y-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine
- Molecular Formula:C22H22N6O
- Molecular Weight:386.456
- Boiling Point:626.3±55.0 °C(Predicted)
- PKA:9.00±0.10(Predicted)
- PSA:90.88000
- Density:1.39±0.1 g/cm3(Predicted)
- LogP:4.70230
3-(4-Phenoxy-phenyl)-1-piperidin-3-yl-1H-pyrazolo[3,4-d]pyriMidin-4-ylaMine(Cas 1022150-12-4) Usage
InChI:InChI=1S/C22H22N6O/c23-21-19-20(15-8-10-18(11-9-15)29-17-6-2-1-3-7-17)27-28(22(19)26-14-25-21)16-5-4-12-24-13-16/h1-3,6-11,14,16,24H,4-5,12-13H2,(H2,23,25,26)
1022150-12-4 Relevant articles
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1022150-12-4 Process route
-
-
(R)-1-(1-benzylpiperidin-3-yl)-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
-
-
1022150-12-4
(R)-3-(4-phenoxyphenyl)-1-(piperidine-3-yl)-1H-pyrazolo[3,4-d]pyrimidine-4-amine
| Conditions | Yield |
|---|---|
|
With
hydrogen;
In
methanol; water;
at 50 ℃;
for 2h;
under 1034.32 Torr;
Acidic conditions;
|
67.4% |
|
With
hydrogenchloride; 10 wt% Pd(OH)2 on carbon;
In
methanol;
at 40 - 50 ℃;
|
|
|
With
palladium 10% on activated carbon; hydrogen;
In
methanol;
|
-
-
330786-24-8
3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
-
-
143900-44-1
tert-butyl (3S)-3-hydroxypiperidine-1-carboxylate
-
-
1022150-12-4
(R)-3-(4-phenoxyphenyl)-1-(piperidine-3-yl)-1H-pyrazolo[3,4-d]pyrimidine-4-amine
| Conditions | Yield |
|---|---|
|
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
at 25 ℃;
Temperature;
Inert atmosphere;
Large scale;
|
85% |
|
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
at 0 - 30 ℃;
for 25h;
Concentration;
Temperature;
|
80.45% |
|
3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine; tert-butyl (3S)-3-hydroxypiperidine-1-carboxylate;
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
at 20 ℃;
for 5h;
With
hydrogenchloride;
In
tetrahydrofuran; water;
at 20 ℃;
for 5h;
|
69% |
|
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
at 20 ℃;
for 24h;
|
52% |
|
3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine; tert-butyl (3S)-3-hydroxypiperidine-1-carboxylate;
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
at 25 ℃;
for 5.5h;
With
hydrogenchloride;
at 15 ℃;
for 2.5h;
|
45% |
|
Multi-step reaction with 2 steps
1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 1 h / 0 - 50 °C
1.2: 20 h / 50 °C
2.1: hydrogenchloride / tetrahydrofuran; water / 2 h / 50 °C
With
hydrogenchloride; di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran; water;
|
1022150-12-4 Upstream products
-
1022150-11-3
(3R)‐4‐amino‐3‐(4-phenoxyphenyl)‐1‐(1‐tert-butoxycarbonylpiperidine-3-yl)-1H-pyrazolo[3,4-d]pyrimidine
-
151266-23-8
4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidine
-
2380-63-4
4-Aminopyrazolo<3,4-d>pyrimidin
-
1276110-38-3
(R)-3-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carboxylic acid tert-butyl ester
1022150-12-4 Downstream products
-
1412418-18-8
(R)-2-(3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carbonyl)-3-cyclopropylacrylonitrile
-
1412418-65-5
(R)-2-(3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carbonyl)-4,4-dimethylpent-2-enenitrile
-
936563-87-0
ibrutinib
-
1710768-30-1
(R,E)-1-(3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]-pyrimidin-1-yl)piperidin-1-yl)-4-(4-(2-aminoethyl)piperazin-1-yl)but-2-en-1-one
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