ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate

Base Information

Chemical Name:ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate
CAS No.:1309436-41-6
Molecular Formula:C₃₁H₃₇FN₂O₄S
Molecular Weight:552.71
Hs Code.:

Synonyms:ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate

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Chemical Property of ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate

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Technology Process of ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate

There total 11 articles about ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate 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: 33.0%

: 1309435-89-9
ethyl 3-[2-fluoro-4-[[5-(hydroxymethyl)-4-methoxy-2-thienyl]methoxy]phenyl]propanoate

: 208932-96-1
1-methylspiro[indoline-3,4’-piperidine]

: 1309436-41-6
ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate

Guidance literature:: With methanol; sodium cyanoborohydride; at 0 - 20 ℃; for 12h;

Reference yield:

: 100-63-0
phenylhydrazine

: 1309436-41-6
ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluoroacetic acid / toluene; acetonitrile / 35 °C

1.2: 0.75 h / 0 °C

2.1: sodium cyanoborohydride; acetic acid / water; methanol / 8 h / 0 - 20 °C

2.2: pH 8

3.1: hydrogen / 20 % Pd(OH)2/C / methanol / 16 h

4.1: sodium cyanoborohydride; methanol / 12 h / 0 - 20 °C

With methanol; hydrogen; sodium cyanoborohydride; acetic acid; trifluoroacetic acid; 20 % Pd(OH)2/C; In methanol; water; toluene; acetonitrile;

Reference yield:

: 138163-08-3
N-(benzyloxycarbonyl)piperidine-4-carboxaldehyde

: 1309436-41-6
ethyl 3-[2-fluoro-4-[[4-methoxy-5-[(1-methylspiro[indoline-3,4'-piperidine]-1'-yl)methyl]-2-thienyl]methoxy]phenyl]propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluoroacetic acid / toluene; acetonitrile / 35 °C

1.2: 0.75 h / 0 °C

2.1: sodium cyanoborohydride; acetic acid / water; methanol / 8 h / 0 - 20 °C

2.2: pH 8

3.1: hydrogen / 20 % Pd(OH)2/C / methanol / 16 h

4.1: sodium cyanoborohydride; methanol / 12 h / 0 - 20 °C

With methanol; hydrogen; sodium cyanoborohydride; acetic acid; trifluoroacetic acid; 20 % Pd(OH)2/C; In methanol; water; toluene; acetonitrile;