tert-butyl N-((3-aminophenyl)methyl)carbamate → HCID 178453060, compound

HRID 24789Notes

Reaction equation

HRID 24789 reaction equation
C([N:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11](=[C:18](Cl)[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:10]1=[O:26])(=O)C1C=CC=CC=1.[C:27]([O:31][C:32]([NH:34][CH2:35][C:36]1[CH:37]=[C:38]([CH:40]=[CH:41][CH:42]=1)[NH2:39])=[O:33])([CH3:30])([CH3:29])[CH3:28]>C(N(CC)CC)C>[C:27]([O:31][C:32]([NH:34][CH2:35][C:36]1[CH:37]=[C:38]([NH:39]/[C:18](=[C:11]2\[C:10](=[O:26])[NH:9][C:17]3[C:12]\2=[CH:13][CH:14]=[CH:15][CH:16]=3)/[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH:40]=[CH:41][CH:42]=1)=[O:33])([CH3:30])([CH3:28])[CH3:29]

Participants

4

Procedure

Prepared analogously to Example 9 from 1-benzoyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinone and 3-tert.butoxycarbonylaminomethyl-aniline in triethylamine.

Sources & evidence

ORD record
ord-de6efc02e9bf45faa30b11f923455542
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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