Dimethylformamide → HCID 136649844, compound

HRID 1695057Notes

Reaction equation

HRID 1695057 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2C(=[CH:9][CH:10]=1)NC(=O)[C:5]2=[N:12][N:13]=CC1(C)CC(C)(C(O)=O)CN1.Cl.C(N=C=NCCCN(C)C)C.[OH:37][C:38]1C2N=NNC=2[CH:41]=[CH:40][CH:39]=1.C([N:49]([CH2:52][CH3:53])[CH2:50][CH3:51])C.[NH2:54][C:55]1[CH:60]=[C:59]([O:61][CH3:62])[CH:58]=[CH:57][C:56]=1[NH:63][C:64](=[O:75])[C:65]1[CH:70]=[CH:69][C:68]([NH:71][CH2:72][CH2:73][NH2:74])=[N:67][CH:66]=1.[CH3:76][N:77]([CH:79]=[O:80])C>[Cl-].[Na+].O>[NH2:54][C:55]1[CH:60]=[C:59]([O:61][CH3:62])[CH:58]=[CH:57][C:56]=1[NH:63][C:64](=[O:75])[C:65]1[CH:70]=[CH:69][C:68]([NH:71][CH2:72][CH2:73][NH:74][C:38]([C:39]2[C:40]([CH3:41])=[C:52]([CH:53]=[N:13][N:12]=[C:5]3[C:4]4[C:76](=[CH:9][CH:10]=[C:2]([F:1])[CH:3]=4)[NH:77][C:79]3=[O:80])[NH:49][C:50]=2[CH3:51])=[O:37])=[N:67][CH:66]=1

Participants

8

Procedure

2-(((5-Fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-4-carboxylic acid (328 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (384 mg, 2 mmol), hydroxybenzotriazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and N-(2-amino-4-methoxyphenyl)-6-(2-aminoethylamino)nicotinamide (316 mg, 1.05 mmol) were added. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with 400 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (397 mg, 65%) as a red solid. LC-MS (m/z) 612 (M+1).

Workup

  1. additionwere added
  2. filtrationThe solids were collected by vacuum filtration
  3. washwashed with water
  4. customdried under vacuum

Sources & evidence

ORD record
ord-377e05851c134a3fbda789405d7c1887
Source dataset
uspto-grants-2012_04
Patent number
US08158656B2

Reaction notes

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