Triethylamine → HCID 178473978, compound

HRID 1728495Notes

Reaction equation

HRID 1728495 reaction equation
ClC(OCC)=O.[C:7]([C@@H:10]1[N:13]([C:14](=[O:16])[CH3:15])[C:12](=[O:17])[C@H:11]1[CH2:18][CH2:19][CH2:20][NH:21][C:22]([NH:34][C:35]([O:37][CH2:38][C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)=[O:36])=[N:23][C:24]([O:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[O:25])([OH:9])=O.C(N(CC)CC)C.Cl.[CH2:53]([O:60][C:61](=[O:64])[CH2:62][NH2:63])[C:54]1[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=1>C(Cl)Cl>[O:64]=[C:61]([O:60][CH2:53][C:54]1[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=1)[CH2:62][NH:63][C:7]([C@@H:10]1[N:13]([C:14](=[O:16])[CH3:15])[C:12](=[O:17])[C@H:11]1[CH2:18][CH2:19][CH2:20][NH:21][C:22]([NH:34][C:35]([O:37][CH2:38][C:39]1[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=1)=[O:36])=[N:23][C:24]([O:26][CH2:27][C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1)=[O:25])=[O:9]

Participants

6

Reactant 4

HCID 8471Triethylamine2×HCID 10928Ethyl chloroformateHCID 11701227Benzyl 2-aminoacetate hydrochlorideHCID 178473979HCID 178473979, compound

Product 1

HCID 178473978HCID 178473978, compoundYield 47%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

To a -10° C. methylene chloride (2 mL) solution of ethyl chloroformate (57 mg, 0.53 mmol) was added a methylene chloride (2 mL) solution of compound 29 (220 mg, 0.44 mmol) and triethylamine (530 mg, 0.13 mmol). The resultant solution was stirred between -5° C. and 5° C. for 1 h. Glycine benzyl ester hydrochloride (O.11 g, 0.64) was added, followed by triethylamine (0.53 g, 0.13 mmol). The resulting suspension was stirred at room temperature for 21 h and filtered through a sintered glass funnel. The solid was washed with methylene chloride. The filtrate and the washing portion were combined and washed with 1N HCl, dried (MgSO4), and concentrated. The residue was purified by silica gel chromatography (Et2O:EtOAc/9:1) to afford 140 mg (47% of the title product.

Workup

  1. addition11 g, 0.64) was added
  2. filtrationfiltered through a sintered glass funnel
  3. washThe solid was washed with methylene chloride
  4. washwashed with 1N HCl
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel chromatography (Et2O:EtOAc/9:1)

Sources & evidence

ORD record
ord-8b161930d5264383b04b98b7076f55a9
Source dataset
uspto-grants-1994_07
Patent number
US05326863

Reaction notes

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