Ethyl 6-hydroxy-7-(prop-2-en-1-yl)-1H-indole-2-carboxylate → HCID 20183534, compound

HRID 255508Notes

Reaction equation

HRID 255508 reaction equation
[OH:1][C:2]1[C:10]([CH2:11][CH:12]=[CH2:13])=[C:9]2[C:5]([CH:6]=[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[NH:8]2)=[CH:4][CH:3]=1>C(O)C.[Pd]>[OH:1][C:2]1[C:10]([CH2:11][CH2:12][CH3:13])=[C:9]2[C:5]([CH:6]=[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[NH:8]2)=[CH:4][CH:3]=1

Participants

4

Procedure

The product of step b) was dissolved in dry ethanol (350 ml), treated with 10% Pd/C (0.3 g) and hydrogenated at 35 psi at room temperature until H2 uptake ceased (1.5 hours). The catalyst was filtered off and the filtrate evaporated to dryness.

Workup

  1. custom(1.5 hours)
  2. filtrationThe catalyst was filtered off
  3. customthe filtrate evaporated to dryness

Sources & evidence

ORD record
ord-15372c7080454dc689a6f0ecb4b3b457
Source dataset
uspto-grants-1987_10
Patent number
US04698345

Reaction notes

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