1,2-Benzenediol, 4-(2-amino-1-hydroxyethyl)- → HCID 131726384, compound

HRID 1349242

Reaction equation

HRID 1349242 reaction equation
C(O[C:6]([N:8]1[CH2:12][C:11](=[N:13][O:14][CH3:15])[CH2:10][C@H:9]1[C:16]([OH:18])=O)=[O:7])(C)(C)C.[C:19]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH:24]=[CH:23][C:22](C(Cl)=O)=[CH:21][CH:20]=1.[NH2:34][CH2:35][CH:36]([C:38]1[CH:39]=[C:40]([OH:45])[C:41]([OH:44])=[CH:42][CH:43]=1)[OH:37]>>[C:28]1([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH:29]=[CH:30][C:31]([C:6]([N:8]2[CH2:12][C:11](=[N:13][O:14][CH3:15])[CH2:10][CH:9]2[C:16]([NH:34][CH2:35][CH:36]([C:38]2[CH:43]=[CH:42][C:41]([OH:44])=[C:40]([OH:45])[CH:39]=2)[OH:37])=[O:18])=[O:7])=[CH:32][CH:33]=1

Participants

4

Reactant 3

HCID 9511,2-Benzenediol, 4-(2-amino-1-hydroxyethyl)-HCID 841514-Phenylbenzoyl chlorideHCID 58714586(2S,4EZ)-1(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid

Product 1

HCID 131726384HCID 131726384, compound

Procedure

Following the general method as outlined in Example 22, starting from (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid, [1,1′-biphenyl]-4-carbonyl chloride, and 4-[(1RS)-2-amino-1-hydroxyethyl]-1,2-benzenediol, the title compound was obtained in 66% purity by HPLC. MS(ESI+): m/z=490.

Sources & evidence

ORD record
ord-9131700a2fb34a4f91c51b702f009bdc
Source dataset
uspto-grants-2007_05
Patent number
US07211601B2

Linked notes

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