Triethylamine → HCID 86627647, compound

HRID 599397Notes

Reaction equation

HRID 599397 reaction equation
C(N(CC)CC)C.[OH:8][N:9]1[C:13](=[O:14])[C:12]2=[CH:15][CH:16]=[CH:17][CH:18]=[C:11]2[C:10]1=[O:19].[C:20]([O:24][C:25](=[O:46])[NH:26][CH2:27][CH2:28][CH2:29][N:30]1[C:42]2[C:41]3[CH:40]=[CH:39][CH:38]=[CH:37][C:36]=3[N:35]=[C:34]([NH2:43])[C:33]=2[N:32]=[C:31]1[CH2:44]Cl)([CH3:23])([CH3:22])[CH3:21]>CN(C=O)C.O>[NH2:43][C:34]1[C:33]2[N:32]=[C:31]([CH2:44][O:8][N:9]3[C:10](=[O:19])[C:11]4[C:12](=[CH:15][CH:16]=[CH:17][CH:18]=4)[C:13]3=[O:14])[N:30]([CH2:29][CH2:28][CH2:27][NH:26][C:25](=[O:46])[O:24][C:20]([CH3:21])([CH3:23])[CH3:22])[C:42]=2[C:41]2[CH:40]=[CH:39][CH:38]=[CH:37][C:36]=2[N:35]=1

Participants

6

Procedure

Triethylamine (4.6 mL, 33.1 mmol) was added to a solution of N-hydroxyphthalimide (2.16 g, 13.2 mmol) in DMF (10 mL). A solution of tert-butyl[3-(4-amino-2-chloromethyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]carbamate (4.3 g, 11.0 mmol) in DMF (20 ml) was added. The reaction was stirred at ambient temperature for 3.5 hours and then diluted with water (100 mL). The resulting precipitate was isolated by filtration, washed with water, and then dried in a vacuum oven at 60° C. over the weekend to provide 4.25 g of tert-butyl (3-{4-amino-2-[(1,3-dioxo-1,3-dihydroisoindol-2-yl)oxymethyl]-1H-imidazo[4,5-c]quinolin-1-yl}propyl)carbamate as a light yellow solid.

Workup

  1. customThe resulting precipitate was isolated by filtration
  2. washwashed with water
  3. customdried in a vacuum oven at 60° C. over the weekend

Sources & evidence

ORD record
ord-0394ce2c0112486486e81db1cda6a671
Source dataset
uspto-grants-2011_03
Patent number
US07897767B2

Reaction notes

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