1-Hydroxybenzotriazole → 1-Acetyl-piperidine-4-carboxylic acid {3-[5-(2-bromo-3-methyl-benzoyl)-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl]-propyl}-(3-chloro-4-methyl-phenyl)-amide

HRID 2236055Notes

Reaction equation

HRID 2236055 reaction equation
[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.N=C=N.C1C=CC2N(O)N=NC=2C=1.[Cl:25][C:26]1[CH:27]=[C:28]([N:33]([CH2:45][CH2:46][CH2:47][N:48]2[CH2:55][CH:54]3[CH:50]([CH2:51][NH:52][CH2:53]3)[CH2:49]2)[C:34]([CH:36]2[CH2:41][CH2:40][N:39]([C:42](=[O:44])[CH3:43])[CH2:38][CH2:37]2)=[O:35])[CH:29]=[CH:30][C:31]=1[CH3:32].CCN(C(C)C)C(C)C>C(Cl)Cl.CN(C=O)C>[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([N:52]1[CH2:53][CH:54]2[CH2:55][N:48]([CH2:47][CH2:46][CH2:45][N:33]([C:28]3[CH:29]=[CH:30][C:31]([CH3:32])=[C:26]([Cl:25])[CH:27]=3)[C:34]([CH:36]3[CH2:37][CH2:38][N:39]([C:42](=[O:44])[CH3:43])[CH2:40][CH2:41]3)=[O:35])[CH2:49][CH:50]2[CH2:51]1)=[O:6]

Participants

8

Reactant 5

HCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 160435CarbodiimideHCID 27355882-Bromo-3-methylbenzoic acidHCID 58782555HCID 58782555, compound

Product 1

HCID 587825071-Acetyl-piperidine-4-carboxylic acid {3-[5-(2-bromo-3-methyl-benzoyl)-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl]-propyl}-(3-chloro-4-methyl-phenyl)-amide

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 6344DichloromethaneSolvent2×

Procedure

A mixture of 2-bromo-3-methyl-benzoic acid (62, 0.016 g, 0.075 mmol), resin-bound carbodiimide (0.078 g, 0.15 mmol) and HOBT (0.012 g, 0.085 mmol) in DCM:DMF (1 mL, 10:1) was shaken for 18 h. A solution of 42b (0.022 g, 0.05 mmol) and DIPEA (0.03 mL, 0.17 mmol) and DCM (1 mL) was added. Shaking was continued for 24 h, the resin filtered and washed with DMF (1 mL) and twice with DCM (1 mL). The reaction mixture was concentrated in vacuo and purified by reverse phase HPLC to afford II-244: ms (ES+) m/z 644 (M+H)+.

Workup

  1. filtrationthe resin filtered
  2. washwashed with DMF (1 mL) and twice with DCM (1 mL)
  3. concentrationThe reaction mixture was concentrated in vacuo
  4. custompurified by reverse phase HPLC
  5. customto afford II-244: ms (ES+) m/z 644 (M+H)+

Sources & evidence

ORD record
ord-cd94cb9874344de4ba14724d7c645da9
Source dataset
uspto-grants-2010_05
Patent number
US07714018B2

Reaction notes

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