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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723771Generated: October 27, 2026

3-Bromo-1-propanol → 3-(4-Fluorobenzoyl)-1,1-dimethyl-8-(2-morpholin-4-YL-ethoxy)-1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1723771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1-propanolHCID 12308—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(3,4-Difluoro-benzoyl)-1,1-dimethyl-8-(3-hydroxy-propoxy)-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl esterHCID 57467958—
Reactant3-(4-Fluorobenzoyl)-8-hydroxy-1,1-dimethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl esterHCID 66640979—
SolventAcetonitrileHCID 6342—
Product3-(4-Fluorobenzoyl)-1,1-dimethyl-8-(2-morpholin-4-YL-ethoxy)-1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylic acid ethyl esterHCID 57467955—

Reaction Conditions

Temperature75 °C

Reaction Steps

To prepare 3-(3,4-difluoro-benzoyl)-1,1-dimethyl-8-(3-hydroxy-propoxy)-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester, A mixture of 3-(4-fluorobenzoyl)-8-hydroxy-1,1-dimethyl-1,2,3,6-tetrahydroazepino[4,5-b]-indole-5-carboxylic acid ethyl ester (46 mg, 0.11 mmol), diisopropylethylamine (0.5 mL), and 3-bromo-1-propanol (1.4 mL) in dry acetonitrile (1 mL) was stirred at 75° C. for 10 hours. The solvent was removed in vacuo, and the residue was purified by preparative reverse-phase HPLC, which was then acylated in the manner described in Example 2A. 1HNMR (CDCl3): δ 10.51 (1H, s), 7.86 (1H, s), 7.82 (1H, d), 7.66-7.59 (2H, m), 7.15-7.09 (2H, m), 6.87 (1H, d), 6.74 (1H, m), 4.27-4.15 (4H, m), 4.09 (2H, br s), 3.90 (2H, m), 2.11-2.05 (2H, m), 1.60 (6H, s), 1.26-1.21 (3H, m). MS (ES): 481 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485634B2
Source datasetuspto-grants-2009_02
ORD IDord-8d5a5e53bf3e41e780ba5e2439e6d448
Source noteuspto-grants-2009_02