HCID 18611289, compound → HCID 57264467, compound

HRID 2413854Notes

Reaction equation

HRID 2413854 reaction equation
S[CH2:2][C:3]([NH:5][C@H:6]([CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C@H:7]([OH:11])[C:8]([OH:10])=[O:9])=O.[C:19](CC(N[C@@H](CC1C=CC=CC=1)[C@H](O)C(O)=O)=S)(=[O:21])[CH3:20].[SH:39]CC(N[C@@H](CC1C=CC=CC=1)[C@H](O)C(O)=O)=O.N[C@H](C(N[C@H](CC1C=CC=CC=1)[C@H](O)C(O)=O)=O)CS.C(CC(N[C@H](CC1C=CC=CC=1)[C@H](O)C(NCC(O)=O)=O)=S)(=O)C.C(CC(N[C@H](CC1C=CC=CC=1)[C@H](O)C(N[C@H](C(O)=O)CC(C)C)=O)=S)(=O)C.C(C(C)C(N[C@H](CC1C=CC=CC=1)[C@H](O)C(O)=O)=S)(=O)C1C=CC=CC=1.C(CCC(N[C@H](CC1C=CC=CC=1)[C@H](O)C(O)=O)=S)(=O)C1C=CC=CC=1>>[C:19]([CH2:2][C:3]([NH:5][C@H:6]([CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C@H:7]([OH:11])[C:8]([OH:10])=[O:9])=[S:39])(=[O:21])[CH3:20]

Participants

9

Reactant 8

HCID 18611289HCID 18611289, compoundHCID 18611290HCID 18611290, compoundHCID 18611292HCID 18611292, compoundHCID 18611293HCID 18611293, compoundHCID 57165755HCID 57165755, compoundHCID 57182890HCID 57182890, compoundHCID 57212220HCID 57212220, compoundHCID 57251419HCID 57251419, compound

Product 1

HCID 57264467HCID 57264467, compound

Procedure

(2S,3R)-3-[N-(mercaptoacetyl)]amino-2-hydroxy-4-phenylbutanoic acid; (2S,3S)-3-[N-(acetylthioacetyl)]amino-2-hydroxy-4-phenylbutanoic acid; (2S,3S)-3[N-(mercaptoacetyl)]amino-2-hydroxy-4-phenylbutanoic acid; (2S,3R)-3-(N-L-cysteinyl)amino-2-hydroxy-4-phenylbutanoic acid; N-{(2S,3R)-3-[N-(acetylthioacetyl)]amino-2-hydroxy-4-phenylbutanoyl}glycine; N-{(2S,3R)-3-[N-(acetylthioacetyl)]amino-2-hydroxy-4-phenylbutanoyl}-L-leucine; (2S,3R)-3-[N-(2-benzoylthiopropionyl)]amino-2-hydroxy-4-phenylbutanoic acid; and (2S,3R)-3-[N-(3-benzoylthiopropionyl)]amino-2-hydroxy-4-phenylbutanoic acid.

Sources & evidence

ORD record
ord-bf09c79eee974c41b5b571ae3d05267b
Source dataset
uspto-grants-1988_01
Patent number
US04719231

Reaction notes

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