Toluene → N-(3,5-Bis(hydroxymethyl)phenyl)-1-((3,4-dichlorophenyl)methyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide

HRID 2170540Notes

Reaction equation

HRID 2170540 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][N:10]2[C:14]([CH3:15])=[C:13]([C:16]([NH:18][C:19]3[CH:20]=[C:21]([C:29](OC)=[O:30])[CH:22]=[C:23]([C:25](OC)=[O:26])[CH:24]=3)=[O:17])[N:12]=[N:11]2)[CH:5]=[CH:6][C:7]=1[Cl:8].CC(C[AlH]CC(C)C)C.C1(C)C=CC=CC=1.[NH4+].[Cl-]>C1COCC1>[OH:26][CH2:25][C:23]1[CH:24]=[C:19]([NH:18][C:16]([C:13]2[N:12]=[N:11][N:10]([CH2:9][C:4]3[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=3)[C:14]=2[CH3:15])=[O:17])[CH:20]=[C:21]([CH2:29][OH:30])[CH:22]=1

Participants

6

Procedure

To a solution of dimethyl 5-[({1-[(3,4-dichlorophenyl)methyl]-5-methyl-1H-1,2,3-triazol-4-yl}carbonyl)amino]-1,3-benzenedicarboxylate (Intermediate 14) (0.65 g, 1.3 mmol) in THF (40 mL), was added a 1M solution of DIBAL-H in toluene (10 mL, 7 eq) and the reaction was stirred to room temperature for 2 hours. Solid NH4Cl was added and the reaction mixture was stirred at RT for 30 min. The aqueous phase was extracted with ether and AcOEt, dried over sodium sulphate and evaporated. After recrystallisation from acetonitrile, the title compound was obtained as a white solid (240 mg, 44%). HRMS calculated for C19H18Cl2N4O3 (M+H)+421.0834. found: 421.0833, Rt: 2.51 min. MP: 194.5° C.

Workup

  1. stirringthe reaction mixture was stirred at RT for 30 min
  2. extractionThe aqueous phase was extracted with ether and AcOEt
  3. dry with materialdried over sodium sulphate
  4. customevaporated
  5. customAfter recrystallisation from acetonitrile

Sources & evidence

ORD record
ord-b0312b67f231460482d00138980796ea
Source dataset
uspto-grants-2015_06
Patent number
US09051281B2

Reaction notes

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