4-Phenylbenzoyl chloride → HCID 58714588, compound

HRID 1242613Notes

Reaction equation

HRID 1242613 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.[O:34]1[CH:38]=[CH:37][CH:36]=[C:35]1[CH2:39][S:40]([CH2:43][C:44](=[N:46]O)[NH2:45])(=[O:42])=[O:41]>>[CH3:15][O:14][N:13]=[C:11]1[CH2:10][C@@H:9]([C:16]2[O:18][N:46]=[C:44]([CH2:43][S:40]([CH2:39][C:35]3[O:34][CH:38]=[CH:37][CH:36]=3)(=[O:42])=[O:41])[N:45]=2)[N:8]([C:6]([C:31]2[CH:30]=[CH:29][C:28]([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)=[CH:33][CH:32]=2)=[O:7])[CH2:12]1

Participants

4

Reactant 3

HCID 841514-Phenylbenzoyl chlorideHCID 28199592-(furan-2-ylmethylsulfonyl)-N'-hydroxyethanimidamideHCID 58714586(2S,4EZ)-1(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid2×

Product 1

HCID 58714588HCID 58714588, compound

Procedure

Following the general method as outlined in Example 59, starting from (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidine-carboxylic acid (Intermediate 2), [1,1′-biphenyl]-4-carbonyl chloride, and 2-[(2-furylmethyl)sulfonyl]-N′-hydroxy-ethanimidamide, the title compound was obtained in 88% purity by HPLC. MS(ESI+): m/z=521.4.

Sources & evidence

ORD record
ord-85ab661ab306486bbf8ba67526a1d917
Source dataset
uspto-grants-2006_10
Patent number
US07115639B2

Reaction notes

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