Dichloromethane → HCID 57732141, compound

HRID 1808170Notes

Reaction equation

HRID 1808170 reaction equation
C(O)(C(F)(F)F)=O.COC1C=C(OC)C=CC=1C[N:13]([C:37]1[S:38][CH:39]=[CH:40][N:41]=1)[S:14]([C:17]1[CH:36]=[CH:35][C:20]([C:21]([NH:23][CH2:24][C:25]2[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=2)=[O:22])=[CH:19][N:18]=1)(=[O:16])=[O:15].C(Cl)Cl.C(N(CC)CC)C>CCOCC>[S:38]1[CH:39]=[CH:40][N:41]=[C:37]1[NH:13][S:14]([C:17]1[CH:36]=[CH:35][C:20]([C:21]([NH:23][CH2:24][C:25]2[CH:30]=[CH:29][C:28]([C:31]([F:33])([F:34])[F:32])=[CH:27][CH:26]=2)=[O:22])=[CH:19][N:18]=1)(=[O:15])=[O:16]

Participants

6

Reactant 4

HCID 6344DichloromethaneHCID 6422Trifluoroacetic acid2×HCID 8471TriethylamineHCID 57732179HCID 57732179, compound

Product 1

HCID 57732141HCID 57732141, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

TFA (750 L, 9.7 mmol) was added to a solution of 6-{[(2,4-dimethoxybenzyl)(1,3-thiazol-2-yl)amino]sulfonyl}-N-[4-(trifluoromethyl)benzyl]nicotinamide (Preparation 88, 1.15 g, 1.94 mmol) in methylene chloride (12 mL, 180 mmol). After 30 min, the reaction mixture was diluted with ether. Triethylamine was added until basic to neutralize the residual TFA. Celite was added, and the mixture was concentrated in vacuo. The residue was purified on the Isco (120 g SiO2 cartridge, chloroform to 12% MeOH in chloroform). The appropriate fractions were concentrated in vacuo. The residue was treated with acetonitrile, generating a white precipitate. The volume was reduced in vacuo, and the solids were collected via filtration, washing with acetonitrile. The off-white product was dried under vacuum (428 mg, 47%).

Workup

  1. additionCelite was added
  2. concentrationthe mixture was concentrated in vacuo
  3. customThe residue was purified on the Isco (120 g SiO2 cartridge, chloroform to 12% MeOH in chloroform)
  4. concentrationThe appropriate fractions were concentrated in vacuo
  5. additionThe residue was treated with acetonitrile
  6. filtrationthe solids were collected via filtration
  7. washwashing with acetonitrile
  8. customThe off-white product was dried under vacuum (428 mg, 47%)

Sources & evidence

ORD record
ord-fde780f1a5944882ac1dd58b95660751
Source dataset
uspto-grants-2013_01
Patent number
US08357711B2

Reaction notes

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