1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile

Base Information

Chemical Name:1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile
CAS No.:132148-54-0
Molecular Formula:C₂₇H₃₁N₃O₂
Molecular Weight:429.562
Hs Code.:

Synonyms:1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile

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Chemical Property of 1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile

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Technology Process of 1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile

There total 4 articles about 1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile 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: 98.0%

: 22311-12-2
N-<β-(5'-Benzyloxy-3'-indolyl)-ethyl>-4-(1-hydroxymethyl-propyl)-pyridiniumbromid

: 132148-54-0
1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile

Guidance literature:: With hydrogenchloride; potassium cyanide; sodium tetrahydroborate; In methanol; diethyl ether; water; for 3.5h; Ambient temperature;
DOI:10.1016/S0040-4020(01)90085-7

Reference yield:

: 41339-61-1
5-benzyloxy-3-(2-hydroxyethyl)indole

: 132148-54-0
1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 51 percent / diethyl ether / 1.) -5 deg C, 1.5 h 2.) refrigerator, overnight;

2: 96 percent

3: 98 percent / 6N HCl, KCN, NaBH₄ / H₂O; diethyl ether; methanol / 3.5 h / Ambient temperature

With hydrogenchloride; potassium cyanide; sodium tetrahydroborate; In methanol; diethyl ether; water;
DOI:10.1016/S0040-4020(01)90085-7

Reference yield:

: 4382-53-0
2-(5-benzyloxy-1H-indol-3-yl)acetic acid

: 132148-54-0
1-[2-(5-Benzyloxy-1H-indol-3-yl)-ethyl]-4-(1-hydroxymethyl-propyl)-1,2,3,6-tetrahydro-pyridine-2-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / LiAlH₄ / tetrahydrofuran / 3.5 h / Ambient temperature

2: 51 percent / diethyl ether / 1.) -5 deg C, 1.5 h 2.) refrigerator, overnight;

3: 96 percent

4: 98 percent / 6N HCl, KCN, NaBH₄ / H₂O; diethyl ether; methanol / 3.5 h / Ambient temperature

With hydrogenchloride; potassium cyanide; sodium tetrahydroborate; lithium aluminium tetrahydride; In tetrahydrofuran; methanol; diethyl ether; water;
DOI:10.1016/S0040-4020(01)90085-7