Toluene → HCID 86615545, compound

HRID 605096Notes

Reaction equation

HRID 605096 reaction equation
[CH2:1]([O:8][C:9]1[CH:38]=[CH:37][C:12]([O:13][C:14]2[CH:22]=[CH:21][C:17]([C:18](O)=[O:19])=[CH:16][C:15]=2[NH:23][C:24]2[C:25]3[CH:33]=[CH:32][C:31]([CH:34]([CH3:36])[CH3:35])=[N:30][C:26]=3[N:27]=[CH:28][N:29]=2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.S(Cl)([Cl:48])=O>>[CH2:1]([O:8][C:9]1[CH:38]=[CH:37][C:12]([O:13][C:14]2[CH:22]=[CH:21][C:17]([C:18]([Cl:48])=[O:19])=[CH:16][C:15]=2[NH:23][C:24]2[C:25]3[CH:33]=[CH:32][C:31]([CH:34]([CH3:36])[CH3:35])=[N:30][C:26]=3[N:27]=[CH:28][N:29]=2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

4

Procedure

A solution of the product from Example 43C (224 mg, 0.443 mmol) in thionyl chloride (2 mL) was refluxed for 1 hour. The mixture was cooled to room temperature, toluene (5 mL) was added and the mixture concentrated under vacuum to provide the title product as a solid.

Workup

  1. concentrationthe mixture concentrated under vacuum

Sources & evidence

ORD record
ord-6bfca08f7c7d49d39a7948b3c4b09c97
Source dataset
uspto-grants-2011_03
Patent number
US07910595B2

Reaction notes

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