HCID 20469086, compound → HCID 20469148, compound

HRID 1388939Notes

Reaction equation

HRID 1388939 reaction equation
C([O:3][C:4](=[O:28])[CH2:5][C:6]1[N:7]([CH3:27])[C:8]([C:17]([C:19]2[N:20]([CH3:26])[C:21]([S:24][CH3:25])=[CH:22][CH:23]=2)=[O:18])=[C:9]([CH3:16])[C:10]=1C(OCC)=O)C.CN1C(C2N(C)C(SC)=CC=2)=C(C)C=C1CC(O)=O>>[CH3:27][N:7]1[C:8]([C:17]([C:19]2[N:20]([CH3:26])[C:21]([S:24][CH3:25])=[CH:22][CH:23]=2)=[O:18])=[C:9]([CH3:16])[CH:10]=[C:6]1[CH2:5][C:4]([OH:28])=[O:3]

Participants

3

Reactant 2

HCID 20469086HCID 20469086, compoundHCID 20469095HCID 20469095, compound

Product 1

HCID 20469148HCID 20469148, compound

Procedure

Following substantially the same procedures as described in Example 7, steps B, C and D, 10 g of ethyl-1,4-dimethyl-5-(1-methyl-5-methylthiopyrrol-2-oyl)-3-ethoxycarbonylpyrrole-2-acetate was converted in three steps to 6.3 g of 1,4-dimethyl-5-(1-methyl-5-methylthiopyrrol-2-yl)pyrrole-2-acetic acid.

Sources & evidence

ORD record
ord-cf359bba492e4009a1a7ff8129629dfa
Source dataset
uspto-grants-1984_02
Patent number
US04434175

Reaction notes

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