Acetic Acid → 4-(4-{[2-(4-Chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-n-{[4-({4-[(2-cyanoethyl)(cyclopropyl)amino]cyclohexyl}amino)-3-nitrophenyl]sulfonyl}-2-(1h-pyrrolo[2,3-b]pyridin-5-yloxy)benzamide

HRID 707025Notes

Reaction equation

HRID 707025 reaction equation
[NH:1]1[C:5]2=[N:6][CH:7]=[C:8]([O:10][C:11]3[CH:39]=[C:38]([N:40]4[CH2:45][CH2:44][N:43]([CH2:46][C:47]5[CH2:52][CH2:51][C:50]([CH3:54])([CH3:53])[CH2:49][C:48]=5[C:55]5[CH:60]=[CH:59][C:58]([Cl:61])=[CH:57][CH:56]=5)[CH2:42][CH2:41]4)[CH:37]=[CH:36][C:12]=3[C:13]([NH:15][S:16]([C:19]3[CH:24]=[CH:23][C:22]([NH:25][CH:26]4[CH2:31][CH2:30][C:29](=O)[CH2:28][CH2:27]4)=[C:21]([N+:33]([O-:35])=[O:34])[CH:20]=3)(=[O:18])=[O:17])=[O:14])[CH:9]=[C:4]2[CH:3]=[CH:2]1.[CH:62]1([NH:65][CH2:66][CH2:67][C:68]#[N:69])[CH2:64][CH2:63]1.C(O)(=O)C.C([BH3-])#N>O1CCCC1>[Cl:61][C:58]1[CH:59]=[CH:60][C:55]([C:48]2[CH2:49][C:50]([CH3:53])([CH3:54])[CH2:51][CH2:52][C:47]=2[CH2:46][N:43]2[CH2:44][CH2:45][N:40]([C:38]3[CH:37]=[CH:36][C:12]([C:13]([NH:15][S:16]([C:19]4[CH:24]=[CH:23][C:22]([NH:25][CH:26]5[CH2:31][CH2:30][CH:29]([N:65]([CH2:66][CH2:67][C:68]#[N:69])[CH:62]6[CH2:64][CH2:63]6)[CH2:28][CH2:27]5)=[C:21]([N+:33]([O-:35])=[O:34])[CH:20]=4)(=[O:18])=[O:17])=[O:14])=[C:11]([O:10][C:8]4[CH:9]=[C:4]5[CH:3]=[CH:2][NH:1][C:5]5=[N:6][CH:7]=4)[CH:39]=3)[CH2:41][CH2:42]2)=[CH:56][CH:57]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 1435373-(Cyclopropylamino)propionitrileHCID 498716Cyano-borohydrideHCID 671271112-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)-4-(4-((2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-enyl)methyl)piperazin-1-yl)-N-(3-nitro-4-(4-oxo cyclohexylamino)phenylsulfonyl)benzamide

Product 1

HCID 498461584-(4-{[2-(4-Chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-n-{[4-({4-[(2-cyanoethyl)(cyclopropyl)amino]cyclohexyl}amino)-3-nitrophenyl]sulfonyl}-2-(1h-pyrrolo[2,3-b]pyridin-5-yloxy)benzamide

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a solution of EXAMPLE 340C (240 mg) and 3-(cyclopropylamino)propanenitrile (62 mg) in tetrahydrofuran (10 mL) was added acetic acid (2 mL) and MP-cyanoborohydride (300 mg, 2.15 mmol/g). The mixture was stirred overnight. The mixture was filtered and concentrated under vacuum and the residue was dissolved in dimethylsulfoxide/methanol (1:1, 10 mL) and loaded on Gilson, C18(100A) 250×121.2 mm (10 micron), with 30% acetonitrile to 65% acetonitrile over 40 minutes. 1H NMR (300 MHz, dimethylsulfoxide-d6) δ 11.66 (s, 1H), 8.55 (dd, 1H), 8.17 (d, 1H), 8.03 (d, 1H), 7.79 (d, 1H), 7.49 (m, 3H), 7.34 (d, 2H), 7.11 (m, 1H), 7.04 (d, 2H), 6.67 (dd, 1H), 6.38 (d, 1H), 6.19 (d, 1H), 4.01 (m, 1H), 3.56 (m, 1H), 3.06 (m, 4H), 2.88 (t, 2H), 2.65 (m, 6H), 2.19 (m, 6H), 2.00 (m, 7H), 1.51 (m, 6H), 0.92 (s, 6H), 0.42 (m, 4H).

Workup

  1. filtrationThe mixture was filtered
  2. concentrationconcentrated under vacuum
  3. dissolutionthe residue was dissolved in dimethylsulfoxide/methanol (1:1, 10 mL)
  4. waitloaded on Gilson, C18(100A) 250×121.2 mm (10 micron), with 30% acetonitrile to 65% acetonitrile over 40 minutes

Sources & evidence

ORD record
ord-38f1a767ae944588bae0c47d3c4eb9c4
Source dataset
uspto-grants-2015_11
Patent number
US09174982B2

Reaction notes

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