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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780263Generated: October 30, 2026

N-Cbz-L-2-amino-4-sulfamoylbutyric acid → (4S)-1-{(2S,3S)-3-[2(S)-Benzyloxycarbonylamino-4-sulfamoylbutyryl]amino-2-hydroxy-4-phenylbutyryl}-4-chloro-N-t-butyl-L-prolinamide

https://huagongshe.com/reaction/1780263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Cbz-L-2-amino-4-sulfamoylbutyric acidHCID 20055593—
Reactant(4S)-1-[(2S,3S)-3-amino-2-hydroxy-4-phenylbutyryl]-4-chloro-N-t-butyl-L-prolinamideHCID 22872716—
Product(4S)-1-{(2S,3S)-3-[2(S)-Benzyloxycarbonylamino-4-sulfamoylbutyryl]amino-2-hydroxy-4-phenylbutyryl}-4-chloro-N-t-butyl-L-prolinamideHCID 2287271577.6%

Reaction Steps

Following a procedure similar to that described in Example 66, but using 122 mg (0.32 mmol) of (4S)-1-[(2S,3S)-3-amino-2-hydroxy-4-phenylbutyryl]-4-chloro-N-t-butyl-L-prolinamide [prepared as described in Preparation 21(b)] and 100 mg (0.32 mmol) of (S)-2-benzyloxycarbonylamino-4-sulfamoylbutyric acid, 169 mg of the title compound were obtained as a colorless powder, melting at 115°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629406
Source datasetuspto-grants-1997_05
ORD IDord-95561927527c4b05b0c313c82af5a052
Source noteuspto-grants-1997_05