Ammonia → HCID 178505127, compound

HRID 989409Notes

Reaction equation

HRID 989409 reaction equation
[C:1]([CH2:4][N:5]([C:10]1[CH:15]=[CH:14][C:13]([NH:16]/[C:17](=[C:24]2\[C:25](=[O:43])[NH:26][C:27]3[C:32]\2=[CH:31][C:30]([NH:33][S:34]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)(=[O:36])=[O:35])=[CH:29][CH:28]=3)/[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:12][CH:11]=1)[S:6]([CH3:9])(=[O:8])=[O:7])(O)=O.C1N=CN(C(N2C=NC=C2)=O)C=1.[NH3:56].[OH2:57]>CN(C=O)C>[NH2:56][C:1]([CH2:4][N:5]([C:10]1[CH:11]=[CH:12][C:13]([NH:16]/[C:17](=[C:24]2\[C:25](=[O:43])[NH:26][C:27]3[C:32]\2=[CH:31][C:30]([NH:33][S:34]([C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)(=[O:36])=[O:35])=[CH:29][CH:28]=3)/[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)=[CH:14][CH:15]=1)[S:6]([CH3:9])(=[O:7])=[O:8])=[O:57]

Participants

6

Procedure

A solution of 250 mg (0.4 mmol) of (Z)-3-[1-(4-(N-carboxymethyl-N-methylsulphonyl-amino)-phenylamino)-1-phenyl-methylidene]-5-phenylsulphonylamino-2-indolinone and 82 mg (0.4 mmol) of CDI in 5 ml of DMF is stirred for 1 hour at 50° C. 1 ml of condensed ammonia is added and the mixture is stirred for 5 hours at ambient temperature. Then water is added. The yellow precipitate is suction filtered, washed with water, a little isopropanol and ether, then dried in vacuo.

Workup

  1. additionis added
  2. filtrationfiltered
  3. washwashed with water
  4. dry with materiala little isopropanol and ether, then dried in vacuo

Sources & evidence

ORD record
ord-2e45ce20f4444b71992b99e04111805d
Source dataset
uspto-grants-2003_10
Patent number
US06638965B2

Reaction notes

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