1,5-Naphthalenedisulfonic acid → HCID 11355034, compound

HRID 1917033Notes

Reaction equation

HRID 1917033 reaction equation
[OH:1][C@H:2]([C:36]1[CH:45]=[CH:44][C:43]([OH:46])=[C:42]2[C:37]=1[CH:38]=[CH:39][C:40](=[O:47])[NH:41]2)[CH2:3][NH:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:14]1[CH2:19][CH2:18][CH:17]([O:20][C:21](=[O:35])[NH:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH2:16][CH2:15]1.[C:48]1([S:62]([OH:65])(=[O:64])=[O:63])[C:57]2[CH:56]=[CH:55][CH:54]=[C:53]([S:58]([OH:61])(=[O:60])=[O:59])[C:52]=2[CH:51]=[CH:50][CH:49]=1>CO>[C:48]1([S:62]([OH:65])(=[O:64])=[O:63])[C:57]2[CH:56]=[CH:55][CH:54]=[C:53]([S:58]([OH:61])(=[O:60])=[O:59])[C:52]=2[CH:51]=[CH:50][CH:49]=1.[OH:1][C@H:2]([C:36]1[CH:45]=[CH:44][C:43]([OH:46])=[C:42]2[C:37]=1[CH:38]=[CH:39][C:40](=[O:47])[NH:41]2)[CH2:3][NH:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:14]1[CH2:15][CH2:16][CH:17]([O:20][C:21](=[O:35])[NH:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH2:18][CH2:19]1

Participants

4

Reactant 2

HCID 66661,5-Naphthalenedisulfonic acidHCID 9874175HCID 9874175, compound

Product 1

HCID 11355034HCID 11355034, compoundYield 80%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Conditions

Temperature
30 °C

Procedure

Biphenyl-2-ylcarbamic acid 1-{9-[(R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethylamino]nonyl}piperidin-4-yl ester (1.0 g, 1.56 mmol, free base) was dissolved in methanol (10 mL; low water content). A solution of naphthalene-1,5-disulfonic acid (0.45 g, 1.56 mmol) in methanol (5 mL; low water content) was added and the reaction mixture was stirred at 30° C. for two hours and then at room temperature overnight (18 h). The resulting thick slurry was filtered and the filtrate cake was washed with methanol (5 mL) and then dried to give the title compound (1.16 g, 80% yield) as off-white crystalline solid.

Workup

  1. customat room temperature
  2. customovernight (18 h)
  3. filtrationThe resulting thick slurry was filtered
  4. washthe filtrate cake was washed with methanol (5 mL)
  5. customdried

Sources & evidence

ORD record
ord-ce52a0fcb17c4fbbb5ea53fd45feade6
Source dataset
uspto-grants-2013_12
Patent number
US08618131B2

Reaction notes

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