Butyl 4-isocyanatobenzoate → HCID 57559150, compound

HRID 1723800Notes

Reaction equation

HRID 1723800 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:12]2[NH:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[C:11]=2[CH2:10][CH2:9][NH:8][CH:7]=1)=[O:5])[CH3:2].[C:20]([C:27]1[CH:32]=[CH:31][C:30]([N:33]=[C:34]=[O:35])=[CH:29][CH:28]=1)([O:22][CH2:23][CH2:24][CH2:25][CH3:26])=[O:21]>>[CH2:1]([O:3][C:4]([C:6]1[C:12]2[NH:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[C:11]=2[CH2:10][CH2:9][N:8]([C:34](=[O:35])[NH:33][C:30]2[CH:29]=[CH:28][C:27]([C:20]([O:22][CH2:23][CH2:24][CH2:25][CH3:26])=[O:21])=[CH:32][CH:31]=2)[CH:7]=1)=[O:5])[CH3:2]

Participants

3

Reactant 2

HCID 4112112Butyl 4-isocyanatobenzoateHCID 57467979Ethyl 1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylate

Product 1

HCID 57559150HCID 57559150, compound

Procedure

The title compound was prepared in a manner similar to that described in Example 72 by using ethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate and 4-(carbobutoxy)phenyl isocyanate (˜2.0 mg); MS (ES): 476 (MH+).

Sources & evidence

ORD record
ord-c685c562beb84853bb9144404c751326
Source dataset
uspto-grants-2009_02
Patent number
US07485634B2

Reaction notes

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