1-Bromopropane → 9-Methyl-1-phenyl-6-propyl-7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole

HRID 647945Notes

Reaction equation

[CH3:1][N:2]1[CH2:23][CH2:22][C:5]2[NH:6][C:7]3[C:12]([C:4]=2[CH2:3]1)=[C:11]1[C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:14][S:15][C:10]1=[CH:9][CH:8]=3.[H-].[Na+].[CH2:26](Br)[CH2:27][CH3:28]>>[CH3:1][N:2]1[CH2:23][CH2:22][C:5]2[N:6]([CH2:26][CH2:27][CH3:28])[C:7]3[C:12]([C:4]=2[CH2:3]1)=[C:11]1[C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:14][S:15][C:10]1=[CH:9][CH:8]=3

Participants

Reactant 3

HCID 78401-Bromopropane

HCID 24758Sodium hydride

HCID 204843049-Methyl-1-phenyl-7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole

Product 1

HCID 204843079-Methyl-1-phenyl-6-propyl-7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole

Procedure

The compound is formed analogously to that described in Example 28, from 4.8 g of 9-methyl-1-phenyl-7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole, NaH and 1.5 ml of propyl bromide. Melting point: 156° C.

Workup

customThe compound is formed analogously to that

Sources & evidence

ORD record: ord-8d7675b80a0142cb962acde8600e8a54
Source dataset: uspto-grants-1983_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04410536

Reaction notes

Loading…