HCID 57842704, compound → 4-(2-(3-(((Benzyloxycarbonyl)(methyl)amino)methyl)phenylcarbamoyloxy)ethyl)-3-methylphenylbromide

HRID 735654Notes

Reaction equation

HRID 735654 reaction equation
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([NH:25][C:26]([O:28][CH2:29][CH2:30][C:31]2[CH:36]=[CH:35][C:34]([Br:37])=[CH:33][C:32]=2[CH3:38])=[O:27])[CH:20]=1)CC(OCC)=O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.N[C:40]1C=C(C=CC=1)CN(C)C(=O)OCC1C=CC=CC=1.BrC1C=CC(CCO)=C(C)C=1>>[CH2:1]([O:8][C:9]([N:11]([CH2:12][C:19]1[CH:20]=[C:21]([NH:25][C:26]([O:28][CH2:29][CH2:30][C:31]2[CH:36]=[CH:35][C:34]([Br:37])=[CH:33][C:32]=2[CH3:38])=[O:27])[CH:22]=[CH:23][CH:24]=1)[CH3:40])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 57842704HCID 57842704, compoundHCID 578428522-(4-Bromo-2-methylphenyl)ethanolHCID 57842860Benzyl 3-aminobenzyl(methyl)carbamate

Product 1

HCID 578428744-(2-(3-(((Benzyloxycarbonyl)(methyl)amino)methyl)phenylcarbamoyloxy)ethyl)-3-methylphenylbromideYield 69%

Procedure

Using a procedure analogous to that used to prepare 34D, 60B (1.6 g, 5.9 mmol) was reacted with 30B to give 60C (2.0 g, 69%) as an oil. MS (ESI) m/z 512.2 (M+H)+.

Sources & evidence

ORD record
ord-1c0c1f234e2a4594ba8ebfc000aadf8d
Source dataset
uspto-grants-2009_09
Patent number
US07592331B2

Reaction notes

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