(2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide

Base Information

• Chemical Name: (2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide
• CAS No.: 1443749-22-1
• Molecular Formula: C₂₈H₃₂Cl₂FN₃O₃
• Molecular Weight: 548.485
• Mol file: 1443749-22-1.mol

Synonyms:

Chemical Property of (2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide

There total 3 articles about (2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

MI-519-51 (1303605-80-2) → (2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide (1443749-22-1)

Guidance literature:

With sodium hydrogencarbonate; In methanol; water; at 20 ℃; for 72h; pH=8 - 9; Inert atmosphere;

DOI:10.1021/jm4005708

Reference yield:

(1R,3S)-3-aminocyclopentan-1-ol (1110772-05-8,167298-58-0) → (2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide (1443749-22-1)

Guidance literature:

Multi-step reaction with 3 steps

1: tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

2: ammonium cerium (IV) nitrate / acetonitrile; water / 1 h / 20 °C / Inert atmosphere

3: sodium hydrogencarbonate / methanol; water / 72 h / 20 °C / pH 8 - 9 / Inert atmosphere

With ammonium cerium (IV) nitrate; sodium hydrogencarbonate; In tetrahydrofuran; methanol; water; acetonitrile;

DOI:10.1021/jm4005708

Reference yield:

(3S,3'S,4'R,6'R,8'S,8a'R)-6-chloro-8'-(3-chloro-2-fluorophenyl)-6'-neopentyl-3',4'-diphenyl-3',4',8',8a'-tetrahydrospiro[indoline-3,7'-pyrrolo[2,1-c][1,4]oxazine]-1',2(6'H)-dione (897365-81-0) → (2'S,3R,4'S,5'R)-6-chloro-4′-(3-chloro-2-fluorophenyl)-N-((1S,3R)-3-hydroxycyclopentyl)-2'-neopentyl-2-oxospiro-[indoline-3,3'-pyrrolidine]-5'-carboxamide (1443749-22-1)

Guidance literature:

Multi-step reaction with 3 steps

1: tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

2: ammonium cerium (IV) nitrate / acetonitrile; water / 1 h / 20 °C / Inert atmosphere

3: sodium hydrogencarbonate / methanol; water / 72 h / 20 °C / pH 8 - 9 / Inert atmosphere

With ammonium cerium (IV) nitrate; sodium hydrogencarbonate; In tetrahydrofuran; methanol; water; acetonitrile;

DOI:10.1021/jm4005708

upstream raw materials:

MI-519-51

(1R,3S)-3-aminocyclopentan-1-ol

(3S,3'S,4'R,6'R,8'S,8a'R)-6-chloro-8'-(3-chloro-2-fluorophenyl)-6'-neopentyl-3',4'-diphenyl-3',4',8',8a'-tetrahydrospiro[indoline-3,7'-pyrrolo[2,1-c][1,4]oxazine]-1',2(6'H)-dione