Triethylamine → HCID 18464582, compound

HRID 2230656Notes

Reaction equation

HRID 2230656 reaction equation
Cl.[CH2:2]([O:4][CH2:5][CH2:6][N:7]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[N:9]=[C:8]1[N:16]1[CH2:22][CH2:21][CH2:20][N:19]([CH2:23][CH2:24][C:25]2([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[CH2:29][CH2:28][NH:27][CH2:26]2)[CH2:18][CH2:17]1)[CH3:3].[CH3:36][O:37][C:38]1[CH:46]=[CH:45][C:44]([CH:47]2[C:51]([CH3:52])=[N:50][NH:49][N:48]2[CH3:53])=[CH:43][C:39]=1[C:40](O)=[O:41].O.ON1C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C.C(N(CC)CC)C>ClCCl.CO.ClCCl>[CH3:36][O:37][C:38]1[CH:46]=[CH:45][C:44]([CH:47]2[C:51]([CH3:52])=[N:50][NH:49][N:48]2[CH3:53])=[CH:43][C:39]=1[C:40]([N:27]1[CH2:28][CH2:29][C:25]([CH2:24][CH2:23][N:19]2[CH2:20][CH2:21][CH2:22][N:16]([C:8]3[N:7]([CH2:6][CH2:5][O:4][CH2:2][CH3:3])[C:11]4[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=4[N:9]=3)[CH2:17][CH2:18]2)([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH2:26]1)=[O:41]

Participants

8

Reactant 5

HCID 8471TriethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 18464413HCID 18464413, compoundHCID 184649573-(2-(4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepan-1-yl)ethyl)-3-phenylpyrrolidine hydrochloric acid

Product 1

HCID 18464582HCID 18464582, compound

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolvent3×HCID 21226129Dichloromethane methanolSolvent2×

Procedure

Combine 3-(2-(4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepan-1-yl)ethyl)-3-phenylpyrrolidine hydrochloric acid salt (prepared from (−)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine (R,R)-di-p-anisoyltartaric acid salt) (0.64 g, 1.2 mmol) and dichloromethane (12 mL). Add 2-methoxy-5-(3,5-dimethyl-4H-triazol-4-yl)benzoic acid (0.3 g, 1.2 mmol), 1-hydroxybenzotriazole hydrate (0.17 g, 1.23 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.29 g, 1.5 mmol), and triethylamine (0.34 mL, 2.4 mmol). After 6 days, dilute the reaction mixture with dichloromethane and extract with a saturated aqueous sodium bicarbonate solution and then brine, dry the organic layer over MgSO4, filter, and concentrate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 10% methanol/dichloromethane and then 20% methanol/dichloromethane to give a residue. Combine the residue and dichloromethane, extract with water and then brine, dry over Na2SO4, and evaporate in vacuo to give the title compound.

Workup

  1. extractionextract with a saturated aqueous sodium bicarbonate solution
  2. dry with materialbrine, dry the organic layer over MgSO4
  3. filtrationfilter
  4. concentrationconcentrate in vacuo
  5. customto give a residue
  6. extractionextract with water
  7. dry with materialbrine, dry over Na2SO4
  8. customevaporate in vacuo

Sources & evidence

ORD record
ord-7e32d798b7d149f9a56d5b506b4ac415
Source dataset
uspto-grants-2002_07
Patent number
US06423704B1

Reaction notes

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