O-Phenylenediamine → HCID 136387969, compound

HRID 251677Notes

Reaction equation

HRID 251677 reaction equation
[F:1][C:2]([F:35])([F:34])[C:3]1[CH:11]=[C:10]2[C:6]([C:7](=[N:13][N:14]=[CH:15][C:16]3[NH:20][C:19]([CH3:21])=[C:18]([C:22]([NH:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]([OH:32])=O)=[O:23])[C:17]=3[CH3:33])[C:8](=[O:12])[NH:9]2)=[CH:5][CH:4]=1.Cl.C(N=C=NCCCN(C)C)C.O[C:49]1[C:57]2[N:56]=N[NH:54][C:53]=2[CH:52]=[CH:51][CH:50]=1.C(N(CC)CC)C.C1(N)C=CC=CC=1N>[Cl-].[Na+].O.CN(C=O)C>[F:35][C:2]([F:1])([F:34])[C:3]1[CH:11]=[C:10]2[C:6]([C:7](=[N:13][N:14]=[CH:15][C:16]3[NH:20][C:19]([CH3:21])=[C:18]([C:22]([NH:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]([NH:54][C:53]4[CH:52]=[CH:51][CH:50]=[CH:49][C:57]=4[NH2:56])=[O:32])=[O:23])[C:17]=3[CH3:33])[C:8](=[O:12])[NH:9]2)=[CH:5][CH:4]=1

Participants

8

Procedure

6-(5-(((6-trifluoromethyl-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-hexanoic acid (491 mg, 1 mmol), and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (394 mg, 2 mmol), hydroxy-benzotriazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and o-phenylenediamine (432 mg, 4 mmol) were added. The mixture was stirred for 24 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 (384 mg, 66% yield) as a red solid. LC-MS (m/z) 582 (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-03bf96494e3346d1be70a2b00c940782
Source dataset
uspto-grants-2011_01
Patent number
US07863315B2

Reaction notes

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