HCID 20281702, compound → HCID 20281711, compound

HRID 463188Notes

Reaction equation

HRID 463188 reaction equation
CS(O[CH2:6][CH2:7][CH2:8][CH2:9][O:10][C:11]1[C:12]([N+:24]([O-:26])=[O:25])=[CH:13][C:14]2[NH:19][C:18](=[O:20])[O:17][C:16]([CH3:22])([CH3:21])[C:15]=2[CH:23]=1)(=O)=O.[SH:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][N:29]=1>>[N:29]1[CH:30]=[CH:31][CH:32]=[CH:33][C:28]=1[S:27][CH2:6][CH2:7][CH2:8][CH2:9][O:10][C:11]1[C:12]([N+:24]([O-:26])=[O:25])=[CH:13][C:14]2[NH:19][C:18](=[O:20])[O:17][C:16]([CH3:21])([CH3:22])[C:15]=2[CH:23]=1

Participants

3

Reactant 2

HCID 20281702HCID 20281702, compoundHCID 178418616HCID 178418616, compound

Product 1

HCID 20281711HCID 20281711, compound

Procedure

Prepared analogously to Example 210 from 6-(4-methanesulfonyloxy-butoxy)-7-nitro-4,4-dimethyl-4H-3,1-benzoxazin-2-one and 2-mercapto-pyridine.

Sources & evidence

ORD record
ord-6a46eadb34ec4462b8efbdcebeb1c97a
Source dataset
uspto-grants-1985_05
Patent number
US04518597

Reaction notes

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