Hydrochloric Acid → HCID 86647621, compound

HRID 571911Notes

Reaction equation

HRID 571911 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:46]=[C:47]([F:49])[CH:48]=1)[CH2:5][C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11](C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[N:10]=[C:9]2[NH:34][C:35](=[O:45])[C:36]1[CH:41]=[C:40]([CH:42]=[O:43])[CH:39]=[CH:38][C:37]=1[F:44].Cl>O1CCOCC1>[F:1][C:2]1[CH:3]=[C:4]([CH:46]=[C:47]([F:49])[CH:48]=1)[CH2:5][C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[NH:11][N:10]=[C:9]2[NH:34][C:35](=[O:45])[C:36]1[CH:41]=[C:40]([CH:42]=[O:43])[CH:39]=[CH:38][C:37]=1[F:44]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 86647620HCID 86647620, compound

Product 1

HCID 86647621HCID 86647621, compoundYield 77%

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent2×

Procedure

N-[5-(3,5-Difluoro-benzyl)-1-trityl-1H-indazol-3-yl]-2-fluoro-5-formyl-benzamide (740 mg, 1.137 mmol) in dry dioxan (25 mL) was treated with 4N HCl in dioxan (2.8 mL). The reaction was stirred at room temperature for two days. The volatile components were evaporated to dryness and the residue was taken up with Et2O (10 mL), stirred for 1 hour, filtered with suction, washed with Et2O (10 mL), dried at 50° C. under vacuum to afford 358 mg of title compound as a white solid in 77% yield.

Workup

  1. customThe volatile components were evaporated to dryness
  2. stirringstirred for 1 hour
  3. filtrationfiltered with suction
  4. washwashed with Et2O (10 mL)
  5. customdried at 50° C. under vacuum

Sources & evidence

ORD record
ord-17884acba6b44aedb3b24d141b865579
Source dataset
uspto-grants-2015_05
Patent number
US09029356B2

Reaction notes

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