Hydrochloric Acid → HCID 68672253, compound

HRID 512947Notes

Reaction equation

HRID 512947 reaction equation
[NH2:1][C:2]1[CH:47]=[C:46]([N:48]2[CH2:53][CH2:52][N:51]([CH3:54])[CH2:50][CH2:49]2)[CH:45]=[CH:44][C:3]=1[C:4]([NH:6][C:7]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([CH2:16][C:17]3[CH:22]=[C:21]([F:23])[CH:20]=[C:19]([F:24])[CH:18]=3)[CH:14]=2)[N:9](C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[N:8]=1)=[O:5].[CH3:55][S:56]([Cl:59])(=[O:58])=[O:57].Cl>ClCCl.N1C=CC=CC=1.O1CCOCC1>[ClH:59].[F:23][C:21]1[CH:22]=[C:17]([CH:18]=[C:19]([F:24])[CH:20]=1)[CH2:16][C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][CH:12]=1)[NH:9][N:8]=[C:7]2[NH:6][C:4](=[O:5])[C:3]1[CH:44]=[CH:45][C:46]([N:48]2[CH2:53][CH2:52][N:51]([CH3:54])[CH2:50][CH2:49]2)=[CH:47][C:2]=1[NH:1][S:56]([CH3:55])(=[O:58])=[O:57]

Participants

7

Reactant 3

HCID 313Hydrochloric AcidHCID 31297Methanesulfonyl chlorideHCID 68671304HCID 68671304, compound

Product 1

HCID 68672253HCID 68672253, compoundYield 63%

Reagents, catalysts & solvents 3

HCID 1049PyridineSolventHCID 6344DichloromethaneSolventHCID 312751,4-DioxaneSolvent2×

Procedure

To a solution of 2-amino-N-[5-(3,5-difluoro-benzyl)-1-trityl-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-benzamide (29 mg, 0.04 mmol) in anhydrous dichloromethane (2 mL) and dry pyridine (0.05 mL), methanesulfonyl chloride (14.7 mg, 0.01 mL, 0.13 mmol) was added and the reaction mixture was stirred at room temperature for 8 hours. The mixture was poured into ice and was extracted with dichloromethane. The organic layer was washed with 0.1N HCl, then with water, dried over anhydrous Na2SO4 and concentrated to yield a crude whitish solid that was suspended in dioxane (1 mL). After adding 4M HCl in dioxane (0.1 mL) the suspension was stirred overnight. After concentration the residue was suspended in diethyl ether/MeOH 1:1, stirred for 20 min., filtered, washed with the same solvent mixture and dried. The desired product was obtained as the hydrochloride (15 mg, 0.025 mmol, 63%).

Workup

  1. additionThe mixture was poured into ice
  2. extractionwas extracted with dichloromethane
  3. washThe organic layer was washed with 0.1N HCl
  4. dry with materialwith water, dried over anhydrous Na2SO4
  5. concentrationconcentrated
  6. customto yield a crude whitish solid
  7. stirringwas stirred overnight
  8. concentrationAfter concentration the residue
  9. stirringstirred for 20 min.
  10. filtrationfiltered
  11. washwashed with the same solvent mixture
  12. customdried

Sources & evidence

ORD record
ord-afdfc77b7b3e4391b80c5df672b775f1
Source dataset
uspto-grants-2015_08
Patent number
US09102662B2

Reaction notes

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