Triethylamine → HCID 46178915, compound

HRID 1890724Notes

Reaction equation

HRID 1890724 reaction equation
[O:1]=[C:2]1[NH:10][C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C@:3]21[CH2:42][C:13]1[CH:14]=[C:15]3[C:20](=[CH:21][C:12]=1[CH2:11]2)[N:19]=[CH:18][C:17]([CH2:22][NH:23][CH2:24][CH:25]([C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)[CH2:26][NH:27][C:28]1([C:33]([OH:35])=O)[CH2:32][CH2:31][CH2:30][CH2:29]1)=[CH:16]3.C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.C(N(CC)CC)C>C1COCC1>[O:35]=[C:33]1[C:28]2([CH2:32][CH2:31][CH2:30][CH2:29]2)[NH:27][CH2:26][CH:25]([C:36]2[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=2)[CH2:24][N:23]1[CH2:22][C:17]1[CH:18]=[N:19][C:20]2[C:15]([CH:16]=1)=[CH:14][C:13]1[CH2:42][C@:3]3([CH2:11][C:12]=1[CH:21]=2)[C:4]1[C:5](=[N:6][CH:7]=[CH:8][CH:9]=1)[NH:10][C:2]3=[O:1]

Participants

6

Procedure

To a solution of 1-{[3-({[(7,5)-2′-oxo-1′,2′,6,8-tetrahydrospiro[cyclopenta[g]quinoline-7,3′-pyrrolo[2,3-b]pyridin]-3-yl]methyl}amino)-2-phenylpropyl]-amino}cyclopentanecarboxylic acid from Step F (30 mg, 0.053 mmol) and HOBt (8.2 mg, 0.053 mmol) in THF (1 mL) were added EDCI (13.3 mg, 0.069 mmol) and triethylamine (19 μL, 0.14 mmol). This solution was stirred at ambient temperature for 18 h. The solution was then concentrated to yield a residue, which was applied to a silica gel column for purification, eluting with a gradient of 1-7% methanol in DCM. Concentration of the fractions containing the product provided the title compound. MS: m/z=544 (M+1). HRMS: m/z=544.2708, calculated m/z=544.2707 for C34H34N5O2.

Workup

  1. concentrationThe solution was then concentrated
  2. customto yield a residue, which
  3. customwas applied to a silica gel column for purification
  4. washeluting with a gradient of 1-7% methanol in DCM
  5. additionConcentration of the fractions containing the product

Sources & evidence

ORD record
ord-dc2b30b4a433428a92edd5fdeef68b74
Source dataset
uspto-grants-2013_08
Patent number
US08507477B2

Reaction notes

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