Methyl pyrrole-2-carboxylate → HCID 70675200, compound

HRID 876084Notes

Reaction equation

HRID 876084 reaction equation
[F:1][C:2]([F:15])([F:14])[N:3]1[CH:7]=[CH:6][CH:5]=[C:4]1[C:8]1[O:12][C:11](S)=[N:10][N:9]=1.F[C:17](F)(F)[N:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[C:23]([NH:25]N)=O.F[C:30](F)(F)N1C=CC=C1C(OC)=O.N1C=CC=C1C(OC)=O>>[N:18]12[CH2:22][CH2:21][CH:20]([CH2:30][CH2:17]1)[N:25]([C:11]1[O:12][C:8]([C:4]3[N:3]([C:2]([F:15])([F:14])[F:1])[CH:7]=[CH:6][CH:5]=3)=[N:9][N:10]=1)[CH2:23][CH2:19]2

Participants

5

Reactant 4

HCID 136930Methyl pyrrole-2-carboxylateHCID 86709244HCID 86709244, compoundHCID 86709245HCID 86709245, compoundHCID 178506353HCID 178506353, compound

Product 1

HCID 70675200HCID 70675200, compound

Procedure

May be prepared according to Methods A-D from 5-[1-(trifluoromethyl)pyrrol-2-yl]-1,3,4-oxadiazole-2-thiol (Method A), from 1-(trifluoromethyl)pyrrole-2-carbohydrazide (Method B), from methyl 1-(trifluoromethyl)pyrrole-2-carboxylate (Method C), and from methyl 1H-pyrrole-2-carboxylate (Method D).

Workup

  1. customMay be prepared

Sources & evidence

ORD record
ord-d14eaf33c7634fb09498b2d52069b62e
Source dataset
uspto-grants-2015_03
Patent number
US08986654B2

Reaction notes

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