HCID 14276396, compound → HCID 14276395, compound

HRID 1193502Notes

Reaction equation

HRID 1193502 reaction equation
C1(CCCC(N2C[C@@H](O)C[C@H]2C(O)=O)=O)C=CC=CC=1.[C:21]1([CH2:27][CH2:28][CH2:29][C:30]([N:32]2[CH2:43][C@@H:42]([OH:44])[CH2:41][C@H:33]2[C:34]([N:36]2[CH2:40][CH2:39][CH2:38][CH2:37]2)=[O:35])=[O:31])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:21]1([CH2:27][CH2:28][CH2:29][C:30]([N:32]2[CH2:43][C@H:42]([OH:44])[CH2:41][C@H:33]2[C:34]([N:36]2[CH2:37][CH2:38][CH2:39][CH2:40]2)=[O:35])=[O:31])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

Participants

3

Reactant 2

HCID 14276396HCID 14276396, compoundHCID 18631233HCID 18631233, compound

Product 1

HCID 14276395HCID 14276395, compound

Procedure

By employing N-(4-phenylbutanoyl)-cis-4-hydroxy-L-proline in place of N-(4-phenylbutanoyl)-trans-4-hydroxy-L-proline in the procedure of Example 1(a) given above, N-[N-(4-phenylbutanoyl)-cis-4-hydroxy-L-prolyl]pyrrolidine (SUAM 14496) was obtained.

Workup

  1. customwas obtained

Sources & evidence

ORD record
ord-2322949bc61c41cb9c738805bfa1aaf5
Source dataset
uspto-grants-1989_03
Patent number
US04810721

Reaction notes

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