(2-Thienylmethyl)amine → HCID 131725451, compound

HRID 1349075Notes

Reaction equation

HRID 1349075 reaction equation
C(O[C:6]([N:8]1[CH2:12][C:11](=[N:13][O:14][CH2:15][C:16]2[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=2)[CH2:10][C@H:9]1[C:24]([OH:26])=O)=[O:7])(C)(C)C.[C:27]1([CH:33]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)C(Cl)=O)[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.[S:43]1[CH:47]=[CH:46][CH:45]=[C:44]1[CH2:48][NH2:49]>>[C:37]1([CH:33]([C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)[C:6]([N:8]2[CH2:12][C:11](=[N:13][O:14][CH2:15][C:16]3[CH:17]=[CH:18][C:19]([O:22][CH3:23])=[CH:20][CH:21]=3)[CH2:10][C@H:9]2[C:24]([NH:49][CH2:48][C:44]2[S:43][CH:47]=[CH:46][CH:45]=2)=[O:26])=[O:7])[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=1

Participants

4

Reactant 3

HCID 34005(2-Thienylmethyl)amineHCID 746372,2-Diphenylacetyl chlorideHCID 58714542HCID 58714542, compound

Product 1

HCID 131725451HCID 131725451, compound

Procedure

Following the general method as outlined in Example 22, starting from (2S,4EZ)-1-(tert-butoxycarbonyl)-4-{[(4-methoxybenzyl)oxy]imino}-2-pyrrolidinecarboxylic acid, diphenylacetyl chloride, and 2-thienylmethylamine the title compound was obtained in 63% purity by LC/MS. MS(ESI+): m/z=554.4.

Sources & evidence

ORD record
ord-3d23758bbccf45e6b1a648703c4b2819
Source dataset
uspto-grants-2007_05
Patent number
US07211601B2

Reaction notes

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