(4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

Base Information

Chemical Name:(4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone
CAS No.:436809-80-2
Molecular Formula:C₂₁H₁₉ClN₂OS
Molecular Weight:382.914
Hs Code.:

(4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4<i>H</i>-thieno[3,2-<i>c</i>]pyridin-5-yl]-methanone

Synonyms:(4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

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Chemical Property of (4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

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Technology Process of (4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

There total 7 articles about (4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone 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: 64.0%

: 436809-79-9
(4-azidomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

: 436809-80-2
(4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; for 3h;
DOI:10.1016/S0968-0896(01)00066-9

Reference yield:

: 1711-02-0
4-iodobenzoic acid chloride

: 436809-80-2
(4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

Guidance literature:: Multi-step reaction with 6 steps

1.1: 86 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

2.1: i-PrMgBr / tetrahydrofuran / 1 h / -15 °C

2.2: 97 percent / tetrahydrofuran / 3 h / -15 °C

3.1: 87 percent / NaBH₄ / methanol / 0.42 h / 0 - 20 °C

4.1: 99 percent / SOCl₂ / CH₂Cl₂ / 1 h / 0 °C

5.1: 100 percent / NaN₃ / dimethylformamide / 24 h / 20 °C

6.1: 64 percent / H₂ / Pd/C / methanol / 3 h / 20 °C

With sodium tetrahydroborate; thionyl chloride; sodium azide; hydrogen; isopropylmagnesium bromide; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(01)00066-9

Reference yield:

: 213462-12-5
4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine

: 436809-80-2
(4-aminomethyl-phenyl)-[4-(4-chloro-phenyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]-methanone

Guidance literature:: Multi-step reaction with 6 steps

1.1: 86 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

2.1: i-PrMgBr / tetrahydrofuran / 1 h / -15 °C

2.2: 97 percent / tetrahydrofuran / 3 h / -15 °C

3.1: 87 percent / NaBH₄ / methanol / 0.42 h / 0 - 20 °C

4.1: 99 percent / SOCl₂ / CH₂Cl₂ / 1 h / 0 °C

5.1: 100 percent / NaN₃ / dimethylformamide / 24 h / 20 °C

6.1: 64 percent / H₂ / Pd/C / methanol / 3 h / 20 °C

With sodium tetrahydroborate; thionyl chloride; sodium azide; hydrogen; isopropylmagnesium bromide; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(01)00066-9