Triethylamine → (1H-benzo[d]imidazol-4-yl)(1-methyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]-1'-yl)methanone

HRID 2204271Notes

Reaction equation

HRID 2204271 reaction equation
[CH3:1][N:2]1[C:6]2[C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:12]=3[O:13][C:14]3([CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)[C:5]=2[CH:4]=[N:3]1.[NH:20]1[C:24]2[CH:25]=[CH:26][CH:27]=[C:28]([C:29](O)=[O:30])[C:23]=2[N:22]=[CH:21]1.C(N(CC)CC)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[OH-].[Na+]>ClCCl>[NH:20]1[C:24]2[CH:25]=[CH:26][CH:27]=[C:28]([C:29]([N:17]3[CH2:18][CH2:19][C:14]4([C:5]5[CH:4]=[N:3][N:2]([CH3:1])[C:6]=5[C:7]5[CH:8]=[CH:9][CH:10]=[CH:11][C:12]=5[O:13]4)[CH2:15][CH2:16]3)=[O:30])[C:23]=2[N:22]=[CH:21]1

Participants

7

Reactant 5

HCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 27717581H-benzimidazole-4-carboxylic acidHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 585507381-Methylspiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]

Product 1

HCID 58550819(1H-benzo[d]imidazol-4-yl)(1-methyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]-1'-yl)methanone

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

To a solution of 1-methylspiro[chromeno[4,3-c]pyrazole-4,4′-piperidine] (211 mg, 0.830 mmol), 1H-benzimidazole-4-carboxylic acid (134 mg, 0.830 mmol) and triethylamine (346 μL, 2.50 mmol) in dichloromethane (2 mL) was added HATU (314 mg, 0.830 mmol) in one portion and the mixture was stirred for 12 hours. The reaction mixture was treated with 1M NaOH (1 mL) for 10 minutes. Dichloromethane (5 mL) was added. The two layers were separated and the aqueous layer was extracted with dichloromethane (2×5 mL). The organic layers were combined, washed with brine, dried over MgSO4, filtered and evaporated to yield a residue that was purified on silica using a gradient of 0.5-30% MeOH in dichloromethane to yield (1H-benzo[d]imidazol-4-yl)(1-methyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4′-piperidine]-1′-yl)methanone. ESI-MS m/z calc. 399.5, found 400.5 (M+1)+. Retention time: 1.12 minutes (4 min run).

Workup

  1. customThe two layers were separated
  2. extractionthe aqueous layer was extracted with dichloromethane (2×5 mL)
  3. washwashed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customto yield a residue that
  8. customwas purified on silica using a gradient of 0.5-30% MeOH in dichloromethane

Sources & evidence

ORD record
ord-8f4044530b3c4619a96bb43f17af6ffa
Source dataset
uspto-grants-2016_06
Patent number
US09365588B2

Reaction notes

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