Hydrochloric Acid → Brinzolamide

HRID 2225474Notes

Reaction equation

HRID 2225474 reaction equation
O[C@H:2]1[C:7]2[CH:8]=[C:9]([S:11]([NH2:14])(=[O:13])=[O:12])[S:10][C:6]=2[S:5](=[O:16])(=[O:15])[N:4]([CH2:17][CH2:18][CH2:19][O:20][CH3:21])[CH2:3]1.CC(C)(C)C([O-])([O-])[O-].[CH2:30]([N:32](CC)CC)[CH3:31].C1(C)C=CC(S(Cl)(=O)=O)=CC=1.C(N)C.Cl>C(#N)C>[CH2:30]([NH:32][C@@H:2]1[C:7]2[CH:8]=[C:9]([S:11]([NH2:14])(=[O:13])=[O:12])[S:10][C:6]=2[S:5](=[O:16])(=[O:15])[N:4]([CH2:17][CH2:18][CH2:19][O:20][CH3:21])[CH2:3]1)[CH3:31]

Participants

8

Reactant 6

HCID 313Hydrochloric AcidHCID 6341EthylamineHCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 15225314(4S)-4-Hydroxy-2-(3-methoxypropyl)-1,1-dioxo-1,2,3,4-tetrahydro-1lambda~6~-thieno[3,2-e][1,2]thiazine-6-sulfonamideHCID 21927715Trimethylorthoacetate

Product 1

HCID 68844Brinzolamide

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Conditions

Temperature
85 °C

Procedure

A 500-mL flask equipped with a reflux condenser was charged with (S)-3,4-dihydro-4-hydroxy-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide (28.5 g, 0.08 mol), acetonitrile (285 mL), and trimethylorthoacetate (23.4 mL, 0.184 mol). The mixture was heated at reflux (85° C.) for 16 hours, after which TLC analysis indicated complete reaction. After cooling for 1 hour, the solvent was removed by rotary evaporation. The residual oil was dissolved in anhydrous tetrahydrofuran (150 mL) and the solution was transferred to a 1-L, 3-necked flask equipped with a thermometer, an addition funnel, and a nitrogen inlet. The solution was cooled to 4° C. under nitrogen and triethylamine (24.5 mL, 0.176 mol) and p-toluenesulfonyl chloride (30.5 g, 0.160 tool) were added sequentially. A precipitate was observed within 5 minutes. The mixture was stirred at 4 to 7° C. for 2 hours, after which TLC analysis indicated complete tosylation. 70% Aqueous ethylamine (260 mL, 2.80 mol) was added dropwise over 30 minutes while the temperature was kept below 15° C. The mixture was stirred at ambient temperature for 18.5 hours before the solution was cooled to 5° C. and concentrated hydrochloric acid (280 mL) was added dropwise over 1 hour while the temperature was kept below 30° C. The solution was extracted with diethyl ether (2×250 mL) and the combined extracts were back extracted with 1M aqueous hydrochloric acid (200 mL). The pH of the aqueous phase was adjusted to 8 using solid sodium bicarbonate causing a white solid to precipitate. After chilling for 2 hour, the solid was collected by filtration and washed with water. TLC analysis of the filtrate indicated that some product was present, so the filtrate was extracted with ethyl acetate. This and additional ethyl acetate was used to dissolve the filter cake and the solution was dried over magnesium sulfate, filtered, stripped of solvent, and dried to a constant weight of 24.0 grams (78%) of crude (R)-3,4-dihydro-4-ethylamino-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide. Material recrystallized from 2-propanol had the following characteristics: mp 125°-127° C.; IR (KBr) 3313, 1355, 1336, 1174, 1156, 1080, 1015, 914, 904, 652 cm-1 ; 1H NMR (DMSO-d6) δ8.01 (s, 2H), 7.65 (s, 1H), 4.10-4.03 (m, 1H), 3.87-3.76 (m, 2H), 3.47-3.33 (m, 4H), 3.22 (s, 3H) partially overlapped by 3.20-3.09 (m, 1H), 2.59-2.49 (m, 2H), 1.86-1.74 (m, 2H), 1.01 (t 3H, J=7 Hz); [α]25312.6 -26.1° (c=1, pH 3 citric acid buffer); Analysis for C12H21N3O5S3 : Calcd: C, 37.58; H, 5.48; N, 10.96. Found: C, 37.66; H, 5.56; N, 10.98.

Workup

  1. customA 500-mL flask equipped with a reflux condenser
  2. temperatureThe mixture was heated
  3. customreaction
  4. temperatureAfter cooling for 1 hour
  5. customthe solvent was removed by rotary evaporation
  6. dissolutionThe residual oil was dissolved in anhydrous tetrahydrofuran (150 mL)
  7. customequipped with a thermometer, an addition funnel, and a nitrogen inlet
  8. temperatureThe solution was cooled to 4° C. under nitrogen
  9. customwas kept below 15° C
  10. stirringThe mixture was stirred at ambient temperature for 18.5 hours before the solution
  11. temperaturewas cooled to 5° C.
  12. customwas kept below 30° C
  13. extractionThe solution was extracted with diethyl ether (2×250 mL)
  14. extractionthe combined extracts were back extracted with 1M aqueous hydrochloric acid (200 mL)
  15. customto precipitate
  16. temperatureAfter chilling for 2 hour
  17. filtrationthe solid was collected by filtration
  18. washwashed with water
  19. extractionwas extracted with ethyl acetate
  20. dissolutionto dissolve the filter cake
  21. dry with materialthe solution was dried over magnesium sulfate
  22. filtrationfiltered
  23. dry with materialdried to a constant weight of 24.0 grams (78%) of crude (R)-3,4-dihydro-4-ethylamino-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide
  24. customMaterial recrystallized from 2-propanol
  25. custom[α]25312.6 -26.1° (c=1, pH 3 citric acid buffer)

Sources & evidence

ORD record
ord-403ceba96e7f48aa80520601f10a5a7f
Source dataset
uspto-grants-1994_09
Patent number
US05344929

Reaction notes

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