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1378391-45-7

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  • Factory Supply tert-butyl (2S,4S)-2-[4-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolidin-2-yl}-1,11-dihydro[2]benzopyrano[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-(metho

    Cas No: 1378391-45-7

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  • (2S,4S)-2-[5-[1,11-Dihydro-2-[(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amino]-3-methyl-1-oxobutyl]-5-methyl-2-pyrrolidinyl][2]benzopyrano[4',3':6,7]naphth[1,2-d]imidazol-9-yl]-1H-imidazol-2-yl]-4-(methoxym

    Cas No: 1378391-45-7

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  • (2S,4S)-2-[5-[1,11-Dihydro-2-[(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)-amino]-3-methyl-1-oxobutyl]-5-methyl-2-pyrrolidinyl][2]benzopyrano[4',3':6,7]naphth[1,2-d]imidazol-9-yl]-1H-imidazol-2-yl]-4-(methoxy

    Cas No: 1378391-45-7

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1378391-45-7 Usage

Description

Velpatasvir intermediate is an essential compound in the synthesis of Velpatasvir, a potent antiviral agent used in the treatment of hepatitis C virus (HCV) infections. It serves as a crucial building block in the development of effective antiviral medications, playing a significant role in the pharmaceutical industry.

Uses

Used in Pharmaceutical Industry:
Velpatasvir intermediate is used as an organic synthesis intermediate for the preparation of peptide analogs as antiviral agents. It is crucial in the development of condensed pentacyclic imidazole derivatives, which are known for their antiviral properties.
Velpatasvir intermediate is also used as a pharmaceutical intermediate, primarily for the synthesis of the active pharmaceutical ingredient (API) Velpatasvir. This API is a key component in the formulation of antiviral drugs that target and treat hepatitis C virus infections, offering a vital contribution to the healthcare sector.

Synthesis

tot-Butyl (2S,4S)-2-[5-(2-{(2S,5S)-l-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolidin-2-yl}- l,ll-dihydroisochromeno[4',3':6,7]naphtho[l,2-d]imidazol-9-yl)-lH-imidazol-2-yl]-4- (methoxymethyl)pyrrolidine-l-carboxylate tert-Butyl (2S,4S)-2-[5-(2- {(2S,5S)-l-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolidin-2- yl} -l ,4,5,l l-tetrahydroisochromeno[4',3':6,7]naphtho[l,2-d]imidazol-9-yl)-lH-imidazol-2-yl]-4- (methoxymethyl)pyrrolidine-l-carboxylate (8.33 g, 1.049 mmol) was suspended in DCM and activated Mn02 (55.0 g, 630 mmol) was added in a single portion. After 13 h, MeOH (200 mL) was added and the slurry was filtered over celite. The filter cake was washed with MeOH (600 mL) and the filtrate was concentrated under reduced pressure. The crude material was purified by silica column chromatography (0% to 45% MeOH/EtOAc) to afford tert-butyl (2S,4S)-2-[5-(2- {(2S,5S)-l-[N- (methoxycarbonyl)-L-valyl] -5 -methylpyrrolidin-2-yl} -1,11- dihydroisochromeno[4',3':6,7]naphtho[l,2-d]imidazol-9-yl)-lH-imidazol-2-yl]-4- (methoxymethyl)pyrrolidine-l-carboxylate (4.85 g, 58%).

Check Digit Verification of cas no

The CAS Registry Mumber 1378391-45-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,8,3,9 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1378391-45:
(9*1)+(8*3)+(7*7)+(6*8)+(5*3)+(4*9)+(3*1)+(2*4)+(1*5)=197
197 % 10 = 7
So 1378391-45-7 is a valid CAS Registry Number.

1378391-45-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4′,3′:6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl(2S,4S)-2-(5-(2-((2S,5S)-1-((methoxycarbonyl)-L-valyl)-5-methylpyrrolidin-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1378391-45-7 SDS

1378391-45-7Upstream product

1378391-45-7Relevant articles and documents

Preparation method of velpatasvir intermediate

-

Paragraph 0025-0036, (2020/05/01)

The invention discloses a preparation method of a velpatasvir intermediate. The method comprises the following steps: dissolving a compound 1 in an organic solvent, adding ammonium acetate and a catalyst, and completing cyclization and oxidation reactions in one step. The method has the advantages of reaction step shortening, simplicity in post-treatment, few three wastes, low production cost, suitableness for industrial production, and substantial social and economic benefits.

Compound used for inhibiting hepatitis C virus, and pharmaceutical applications thereof

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, (2018/04/01)

The invention relates to a compound which is represented by formula I, is used for inhibiting hepatitis C virus, and possesses excellent bioavailability, and a nontoxic pharmaceutically acceptable salt thereof. The compound possesses extremely high inhibition effect on HCV of all genotypes. In the formula I, R is used for representing hydrogen atom, glycyl, L-alanyl, L-leucyl, L-valyl, or L-isoleucyl.

ANTIVIRAL COMPOUNDS

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, (2013/12/03)

The disclosure is related to anti-viral compounds, compositions containing such compounds, and therapeutic methods that include the administration of such compounds, as well as to processes and intermediates useful for preparing such compounds.

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