Ammonium Chloride → HCID 178481998, compound

HRID 1518053Notes

Reaction equation

HRID 1518053 reaction equation
[F:1][C:2]([F:50])([F:49])[C:3]1[CH:4]=[C:5]([CH:42]=[C:43]([C:45]([F:48])([F:47])[F:46])[CH:44]=1)[CH2:6][N:7]([CH2:14][C:15]1[C:16]([N:27]2[CH2:31][CH2:30][CH2:29][C@@H:28]2[C@H:32]2[CH2:37][CH2:36][C@H:35]([CH2:38][C:39](O)=[O:40])[CH2:34][CH2:33]2)=[N:17][C:18]2[C:23]([CH:24]=1)=[CH:22][C:21]([F:25])=[C:20]([F:26])[CH:19]=2)[C:8]1[N:9]=[N:10][N:11]([CH3:13])[N:12]=1.[NH4+].[Cl-].Cl.C([N:56]=C=NCCCN(C)C)C.ON1C2N=CC=CC=2N=N1>CN(C=O)C.CCOC(C)=O.C(N(CC)CC)C>[F:48][C:45]([F:47])([F:46])[C:43]1[CH:42]=[C:5]([CH:4]=[C:3]([C:2]([F:50])([F:49])[F:1])[CH:44]=1)[CH2:6][N:7]([CH2:14][C:15]1[C:16]([N:27]2[CH2:31][CH2:30][CH2:29][C@@H:28]2[C@H:32]2[CH2:37][CH2:36][C@H:35]([CH2:38][C:39]([NH2:56])=[O:40])[CH2:34][CH2:33]2)=[N:17][C:18]2[C:23]([CH:24]=1)=[CH:22][C:21]([F:25])=[C:20]([F:26])[CH:19]=2)[C:8]1[N:9]=[N:10][N:11]([CH3:13])[N:12]=1

Participants

8

Procedure

To a solution of trans-(4-{(R)-1-[3-({N-[3,5-bis(trifluoromethyl)benzyl]-N-(2-methyl-2H-tetrazol-5-yl)amino}methyl)-6,7-difluoroquinolin-2-yl]pyrrolidin-2-yl}cyclohexyl)acetic acid (85 mg, 0.12 mmol) in DMF (3 mL) is added NH4Cl (10 mg, 0.18 mmol), N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC.HCl 41 mg, 0.18 mmol), 1-hydroxy-7-azabenzotriazole (HOAt, 24 mg, 0.18 mmol), and small amount of triethylamine. After stirring for 2 hours at room temperature, the reaction mixture is diluted with EtOAc, washed successively with water and brine, and dried over magnesium sulfate. Evaporation of the solvent and purification by silica gel column using ethyl acetate-hexane affords trans-(4-{(R)-1-[3-({N-[3,5-bis(trifluoromethyl)benzyl]-N-(2-methyl-2H-tetrazol-5-yl)amino}methyl)-6,7-difluoroquinolin-2-yl]pyrrolidin-2-yl}cyclohexyl)acetic acid amide.

Workup

  1. washwashed successively with water and brine
  2. dry with materialdried over magnesium sulfate
  3. customEvaporation of the solvent and purification by silica gel column

Sources & evidence

ORD record
ord-d4393da418434a1b82746b399d8cba90
Source dataset
uspto-grants-2012_07
Patent number
US08232403B2

Reaction notes

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