Triethylamine → HCID 178443962, compound

HRID 1057411Notes

Reaction equation

HRID 1057411 reaction equation
Cl[C:2]1[NH:7][CH:6]([CH3:8])[N:5]=[C:4]2[N:9]([C:17]3[C:22]([CH3:23])=[CH:21][C:20]([CH3:24])=[CH:19][C:18]=3[CH3:25])[C:10]([CH3:16])=[C:11]([C:12](=[O:15])[CH2:13][Cl:14])[C:3]=12.[NH2:26][CH:27]([CH2:31][CH2:32][CH3:33])[CH2:28][CH2:29][CH3:30].C(N(CC)CC)C>C(OCC)(=O)C>[CH3:30][CH2:29][CH2:28][CH:27]([NH:26][C:2]1[NH:7][CH:6]([CH3:8])[N:5]=[C:4]2[N:9]([C:17]3[C:22]([CH3:23])=[CH:21][C:20]([CH3:24])=[CH:19][C:18]=3[CH3:25])[C:10]([CH3:16])=[C:11]([C:12](=[O:15])[CH2:13][Cl:14])[C:3]=12)[CH2:31][CH2:32][CH3:33]

Participants

5

Procedure

A mixture of compound (7) (730 mg, 2 mmol), 4-aminoheptane (250 mg, 2.2 mmol) and triethylamine (250 mg, 2.5 mmol) were stirred at ambient temperature for 16 hours. The solution was diluted with ethyl acetate and washed with brine. The organic layer was dried over sodium sulfate and evaporated to dryness to provide compound (8).

Workup

  1. washwashed with brine
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. customevaporated to dryness

Sources & evidence

ORD record
ord-49c3fda458f544eb83a3d355c2eca5c4
Source dataset
uspto-grants-2003_02
Patent number
US06514982B1

Reaction notes

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