Diisopropylethylamine → HCID 78427899, compound

HRID 514861Notes

Reaction equation

HRID 514861 reaction equation
[CH2:1]([C:5]1([OH:11])[CH2:10][CH2:9][NH:8][CH2:7][CH2:6]1)[CH:2]([CH3:4])[CH3:3].[NH2:12][C:13]1[CH:22]=[CH:21][C:20]2[C:15](=[C:16]([S:23]([NH:26][C:27]3[CH:35]=[CH:34][C:30]([C:31](O)=[O:32])=[CH:29][CH:28]=3)(=[O:25])=[O:24])[CH:17]=[CH:18][CH:19]=2)[N:14]=1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>C(Cl)Cl>[NH2:12][C:13]1[CH:22]=[CH:21][C:20]2[C:15](=[C:16]([S:23]([NH:26][C:27]3[CH:35]=[CH:34][C:30]([C:31]([N:8]4[CH2:7][CH2:6][C:5]([OH:11])([CH2:1][CH:2]([CH3:4])[CH3:3])[CH2:10][CH2:9]4)=[O:32])=[CH:29][CH:28]=3)(=[O:25])=[O:24])[CH:17]=[CH:18][CH:19]=2)[N:14]=1

Participants

6

Procedure

To a mixture of 4-isobutylpiperidin-4-ol (70 mg, 0.44 mmol), 4-(2-aminoquinoline-8-sulfonamido)benzoic acid (100 mg, 0.44 mmol), and HBTU (134 mg, 0.53 mmol) in DCM (5 mL) was added DIPEA (1 mL) dropwise at room temperature, and then the mixture was stirred at room temperature for 1 hour. The resulting mixture was concentrated, purified by a standard method to yield the title compound. 1H NMR (CHLOROFORM-d) δ: 8.10-8.20 (m, 1H), 7.89 (d, J=9.1 Hz, 1H), 7.69-7.82 (m, 1H), 7.06-7.26 (m, 5H), 6.80 (d, J=9.1 Hz, 1H), 5.41 (s, 2H), 4.33 (br. s., 1H), 3.41-3.19 (m., 3H), 1.82 (dt, J=12.9, 6.4 Hz, 1H), 1.63-1.46 (m, 4H), 1.40 (d, J=5.9 Hz, 2H), 0.97 (d, J=6.7 Hz, 6H). LCMS (m/z): 483.7 (M+1)+

Workup

  1. concentrationThe resulting mixture was concentrated
  2. custompurified by a standard method

Sources & evidence

ORD record
ord-a3e755a805e746eeaa06ae69ca49b7e9
Source dataset
uspto-grants-2015_08
Patent number
US09108921B2

Reaction notes

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