methyl 1H-indole-4-carboxylate → HCID 53948440, compound
Reaction equation
[NH:1]1[C:9]2[CH:8]=[CH:7][CH:6]=[C:5]([C:10]([O:12][CH3:13])=[O:11])[C:4]=2[CH:3]=[CH:2]1.[N:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][C:15]=1[CH2:24][O:25][C:26]1[CH:33]=[CH:32][C:29]([CH2:30]Cl)=[CH:28][CH:27]=1>>[CH3:13][O:12][C:10]([C:5]1[C:4]2[CH:3]=[CH:2][N:1]([CH2:30][C:29]3[CH:28]=[CH:27][C:26]([O:25][CH2:24][C:15]4[CH:16]=[CH:17][C:18]5[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=5)[N:14]=4)=[CH:33][CH:32]=3)[C:9]=2[CH:8]=[CH:7][CH:6]=1)=[O:11]Participants
3
Procedure
This compound was prepared from methyl 4-indole carboxylate and 4-(quinolin-2-ylmethoxy)benzyl chloride (Example 1a by the method described in Example 1b part i), m.p. 128°-131° C.
Sources & evidence
- ORD record
- ord-dc15993083184e438f74de75ad00f53b
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05410061
Reaction notes
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