1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 178494692, compound

HRID 579007Notes

Reaction equation

HRID 579007 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][N:12]([C:15]3[CH:23]=[CH:22][C:18]([C:19]([OH:21])=O)=[CH:17][N:16]=3)[C:13]=2[OH:14])=[CH:5][CH:4]=1)#[N:2].CCN=C=NCCCN(C)C.C1C=C2N=NN(O)C2=CC=1.O.CCN(C(C)C)C(C)C.[CH3:55][O:56][CH2:57][C:58]1([NH2:63])[CH2:62][CH2:61][CH2:60][CH2:59]1>CN(C=O)C>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][N:12]([C:15]3[CH:23]=[CH:22][C:18]([C:19]([NH:63][C:58]4([CH2:57][O:56][CH3:55])[CH2:62][CH2:61][CH2:60][CH2:59]4)=[O:21])=[CH:17][N:16]=3)[C:13]=2[OH:14])=[CH:5][CH:4]=1)#[N:2]

Participants

7

Procedure

Combine 6-(4-(4-cyanophenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid (30 mg, 0.098 mmol), EDCI (28.2 mg, 0.147 mmol), and HOBT hydrate (22.50 mg, 0.147 mmol) in DMF (1 mL) and added Hunig's base (50.6 mg, 0.392 mmol). Then 1-(methoxymethyl)cyclopentanamine (19.0 mg, 0.147 mmol) was added and the reaction mixture was stirred at ambient temperature for 20 h. The reaction mixture was purified using HPLC (45-70% ACN in water, TFA-buffered) to give the title compound as a solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.52-1.80 (m, 6 H) 2.00-2.13 (m, 2 H) 3.27 (s, 3H) 3.60 (s, 2H) 7.79 (d, J=8.59 Hz, 2 H) 7.96-8.78 (m, 6 H) 8.79-8.99 (m, 1 H) 13.53 (br. s., 1 H). MS m/z [M+H]+ 418.

Workup

  1. customThe reaction mixture was purified

Sources & evidence

ORD record
ord-5172870f296e4e5d9ec3a38cf276682b
Source dataset
uspto-grants-2015_05
Patent number
US09040522B2

Reaction notes

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