4-Aminophenethyl alcohol → HCID 21876398, compound

HRID 858439Notes

Reaction equation

HRID 858439 reaction equation
[C:1]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][C:12](Cl)=[C:11]([N+:16]([O-:18])=[O:17])[CH:10]=1)(=[O:8])=[O:7])([CH3:4])([CH3:3])[CH3:2].[NH2:19][C:20]1[CH:25]=[CH:24][C:23]([CH2:26][CH2:27][OH:28])=[CH:22][CH:21]=1>>[C:1]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][C:12]([NH:19][C:20]2[CH:25]=[CH:24][C:23]([CH2:26][CH2:27][OH:28])=[CH:22][CH:21]=2)=[C:11]([N+:16]([O-:18])=[O:17])[CH:10]=1)(=[O:8])=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 296613HCID 296613, compound

Product 1

HCID 21876398HCID 21876398, compound

Procedure

The title compound was prepared according to the procedure described in step 3 of Example 1 from N-(tert-butyl)-4-chloro-3-nitrobenzenesulfonamide (step 1) and 4-aminophenylethyl alcohol.

Sources & evidence

ORD record
ord-6d83defe091545e1ae3cd75b2a643872
Source dataset
uspto-grants-2006_12
Patent number
US07148234B2

Reaction notes

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