HCID 22351056, compound → HCID 69793643, compound

HRID 896509Notes

Reaction equation

HRID 896509 reaction equation
[O:1]=[C:2]1[N:6]([CH2:7][CH2:8][O:9][C:10]2[CH:25]=[CH:24][C:13]([CH:14]=[C:15]([C:20]([O:22][CH3:23])=[O:21])[C:16]([O:18][CH3:19])=[O:17])=[CH:12][CH:11]=2)[C:5]2[CH:26]=[CH:27][C:28]([CH:30]=[CH:31][C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)=[CH:29][C:4]=2[S:3]1.ClCCOC1C=CC(CC(C(OC)=O)C(OC)=O)=CC=1>>[O:1]=[C:2]1[N:6]([CH2:7][CH2:8][O:9][C:10]2[CH:25]=[CH:24][C:13]([CH2:14][CH:15]([C:20]([O:22][CH3:23])=[O:21])[C:16]([O:18][CH3:19])=[O:17])=[CH:12][CH:11]=2)[C:5]2[CH:26]=[CH:27][C:28]([CH:30]=[CH:31][C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=3)=[CH:29][C:4]=2[S:3]1

Participants

3

Reactant 2

HCID 22351056HCID 22351056, compoundHCID 85451252HCID 85451252, compound

Product 1

HCID 69793643HCID 69793643, compound

Procedure

The procedure is as in Step B of Example 37 starting from the compound obtained in Example 85, with the replacement of dimethyl 2-[4-(2-chloroethoxy)benzylidene]malonate with dimethyl 2-[4-(2-chloroethoxy)benzyl]malonate.

Sources & evidence

ORD record
ord-4999269fc77f4e4893c849eb8fbd7469
Source dataset
uspto-grants-2005_07
Patent number
US06919362B2

Reaction notes

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