Glycine, N-(phenylsulfonyl) → HCID 66975150, compound

HRID 1022740Notes

Reaction equation

HRID 1022740 reaction equation
[NH2:1][CH2:2][C@H:3]1[C@H:9]([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]([F:17])[CH:11]=2)[O:8][CH2:7][CH2:6][N:5](C(OC(C)(C)C)=O)[CH2:4]1.[C:25]1([S:31]([NH:34][CH2:35][C:36](O)=[O:37])(=[O:33])=[O:32])[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[ClH:16].[Cl:16][C:13]1[CH:14]=[CH:15][C:10]([C@@H:9]2[O:8][CH2:7][CH2:6][NH:5][CH2:4][C@H:3]2[CH2:2][NH:1][C:36](=[O:37])[CH2:35][NH:34][S:31]([C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)(=[O:33])=[O:32])=[CH:11][C:12]=1[F:17]

Participants

3

Reactant 2

HCID 220662Glycine, N-(phenylsulfonyl)HCID 66975002tert-butyl (6R,7R)-6-(aminomethyl)-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylate

Product 1

HCID 66975150HCID 66975150, compound

Procedure

Using tert-butyl (6R,7R)-6-(aminomethyl)-7-(4-chloro-3-fluorophenyl)-1,4-oxazepane-4-carboxylate and N-(phenylsulfonyl)glycine, and by a method similar to that of Example 39, the title compound was obtained.

Sources & evidence

ORD record
ord-6b50ff3e15714f24b9eb3fb755ba3b09
Source dataset
uspto-grants-2014_05
Patent number
US08722662B2

Reaction notes

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