Oclacitinib Maleate

Basic information

  • Product Name:Oclacitinib Maleate
  • CasNo.:1208319-27-0
  • MF:C19H27N5O6S
  • MW:453.51

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:
  • Packing:
  • Throughput:
Inquiry

Product Details

CasNo: 1208319-27-0

MF: C19H27N5O6S

Oclacitinib Maleate API powder factory Customized supply 1208319-27-0 In stock

  • Molecular Formula:C15H23N5O2S.x(C4H4O4)
  • Molecular Weight:453.51
  • PSA:173.96000 
  • LogP:2.68560 

Veterinary API Oclacitinib Maleate 1208319-27-0 Usage

Oclacitinib is labeled to treat atopic dermatitis and itchiness (pruritus) caused by allergies in dogs, though it has also been used to reduce the itchiness and dermatitis caused by flea infestations. Oclacitinib is a Janus kinase (JAK) inhibitor used for control of pruritus in dogs associated with allergic dermatitis and atopic dermatitis. Oclacitinib has a unique mechanism of action that acts to inhibit proinflammatory cytokines. Liaoning Pharmaceutical Innovation Co.,Ltd. has a R&D center, a pilot workshop and a GMP production base. It integrates scientific research, pilot testing and production, and is committed to providing high-quality pharmaceutical chemicals and contract processing services to the world's pharmaceutical companies. As a research-first and customer-centered enterprise, we have always been unremittingly improving the technological innovation system and prioritizing technological innovation. We also use advanced and complete production facilities and a complete quality assurance system to ensure the safe production of high-quality products. . Positive and innovative ideas, dedicated and dedicated employees, and sufficient and reasonable resource allocation are the firm cornerstones that promote the gradual development and growth of Fuyin Technology.

1208319-27-0 Relevant articles

Preparation method of 7H-pyrrolo [2, 3-d] pyrimidine compound

-

Paragraph 0064-0066; 0083-0085, (2021/01/30)

The invention discloses a preparation me...

Preparation method of olatinib maleate

-

Paragraph 0023; 0064-0067; 0080-0082, (2020/11/23)

The invention discloses a preparation me...

SOLID STATE FORMS OF OCLACITINIB MALEATE

-

Page/Page column 13-14, (2020/08/22)

The present invention relates to solid s...

PROCESS FOR PREPARING 7H-PYRROLO[2,3-D]PYRIMIDINE COMPOUNDS

-

Paragraph 0135, (2017/09/02)

Described herein are improved processes ...

1208319-27-0 Process route

Oclacitinib

Oclacitinib

maleic acid
110-16-7,26099-09-2

maleic acid

N-methyl-1-{trans-4-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclohexyl}methanesulfonamide maleate
1208319-27-0,1640292-55-2

N-methyl-1-{trans-4-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclohexyl}methanesulfonamide maleate

Conditions
Conditions Yield
With pyrographite; In ethanol; at 78 - 80 ℃;
95.6%
In water; at 37 - 60 ℃; Temperature;
 
In water; butan-1-ol; at 20 ℃; for 18h;
253.0 g
N-methyl-1-{trans-4-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclohexyl}methanesulfonamide

N-methyl-1-{trans-4-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclohexyl}methanesulfonamide

(2E)-but-2-enedioic acid
110-17-8,26099-09-2

(2E)-but-2-enedioic acid

oclacitinib maleate
1208319-27-0,1640292-55-2

oclacitinib maleate

Conditions
Conditions Yield
With pyrographite; In ethanol; at 78 - 80 ℃;
95.5%

1208319-27-0 Upstream products

  • 110-16-7
    110-16-7

    maleic acid

  • 2124221-12-9
    2124221-12-9

    trans-4-((methylamino)cyclohexyl)methanesulfonic acid

  • 589-15-1
    589-15-1

    1-bromomethyl-4-bromobenzene

  • 4746-97-8
    4746-97-8

    cyclohexanedione monoethylene ketal