Potassium Hydroxide → 7-Chloro-6-(4-trifluoromethoxybenzylthio)-2,3,4,5-tetrahydro-1H-benzo[d]azepine Hydrochloride

Temperature

57.5 °C

To a 4:1 mixture of 3-tert-butoxycarbonyl-7-chloro-6-dimethylcarbamoylthio-2,3,4,5-tetrahydro-1H-benzo[d]azepine and 3-tert-butoxycarbonyl-7,9-dichloro-6-dimethylcarbamoylthio-2,3,4,5-tetrahydro-1H-benzo[d]azepine (102 mg, 0.27 mmol) in methanol (1.7 mL) under nitrogen, add potassium hydroxide (0.9 g, 16.1 mmol) at ambient temperature. When the mixture becomes homogenous, heat at 55-60° C. for 2-3 h, until TLC shows the disappearance of starting material. Cool to ambient temperature, add aqueous saturated ammonium chloride solution, extract three times with diethyl ether, dry over anhydrous MgSO4, and concentrate in vacuo. Dissolve the crude 3-tert-butoxycarbonyl-7-chloro-6-mercapto-2,3,4,5-tetrahydro-1H-benzo[d]azepine in anhydrous DCM (2 mL) under nitrogen. Add with stirring DBU (80 μL, 0.532 mmol) and 4-(trifluoromethoxy)benzyl bromide (77 μL, 0.53 mmol) at ambient temperature and allow the reaction to continue overnight. Dilute with aqueous saturated ammonium chloride solution, extract three times with diethyl ether, dry over anhydrous MgSO4, and concentrate in vacuo. Treat a solution of the crude 3-tert-butoxycarbonyl-7-chloro-6-(4-trifluoromethoxy-benzylthio)-2,3,4,5-tetrahydro-1H-benzo[d]azepine in DCM (2 mL) with 2M hydrogen chloride in ether (excess) and continue stirring until TLC shows consumption of starting material. Concentrate in vacuo and triturate the obtained solid with ether/pentane (10:90). Purify by preparative TLC eluting with 19:1 DCM/saturated ammonia in methanol and convert to the hydrochloride by following a method similar to the General Procedure 2-2 to give the title compound as a white solid (48 mg, 43%). MS (APCI+) m/z: 388 (M+H)+.

1. temperatureCool to ambient temperature
2. extractionextract three times with diethyl ether
3. dry with materialdry over anhydrous MgSO4
4. concentrationconcentrate in vacuo
5. dissolutionDissolve the crude 3-tert-butoxycarbonyl-7-chloro-6-mercapto-2,3,4,5-tetrahydro-1H-benzo[d]azepine in anhydrous DCM (2 mL) under nitrogen
6. customthe reaction
7. extractionextract three times with diethyl ether
8. dry with materialdry over anhydrous MgSO4
9. concentrationconcentrate in vacuo
10. additionTreat a solution of the crude 3-tert-butoxycarbonyl-7-chloro-6-(4-trifluoromethoxy-benzylthio)-2,3,4,5-tetrahydro-1H-benzo[d]azepine in DCM (2 mL) with 2M hydrogen chloride in ether (excess)
11. customconsumption of starting material
12. concentrationConcentrate in vacuo
13. customtriturate the obtained solid with ether/pentane (10:90)
14. customPurify by preparative TLC
15. washeluting with 19:1 DCM/saturated ammonia in methanol

ORD record

ord-4c1d1400ccef4bb0b8c66c757db4769f

Source dataset

uspto-grants-2011_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08022062B2