Sulfanilamide → HCID 15712767, compound

HRID 703772Notes

Reaction equation

HRID 703772 reaction equation
[C:1]([NH:11][CH:12]([C:17]([OH:19])=O)[CH2:13][CH:14]([CH3:16])[CH3:15])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].[NH2:20][C:21]1[CH:26]=[CH:25][C:24]([S:27]([NH2:30])(=[O:29])=[O:28])=[CH:23][CH:22]=1>>[C:1]([NH:11][CH:12]([C:17]([NH:20][C:21]1[CH:26]=[CH:25][C:24]([S:27]([NH2:30])(=[O:28])=[O:29])=[CH:23][CH:22]=1)=[O:19])[CH2:13][CH:14]([CH3:15])[CH3:16])([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2]

Participants

3

Reactant 2

HCID 5333SulfanilamideHCID 2466732-(((Benzyloxy)carbonyl)amino)-4-methylpentanoic acid

Product 1

HCID 15712767HCID 15712767, compound

Procedure

Observing the procedure of Example I, N-carbobenzyloxy-DL-leucine is reacted with 4-amino-benzenesulfonamide to yield the desired product, 4-(N-carbobenzyloxy-DL-leucylamino)benzene-sulfonamide having a mp. of 167°-8° C.

Sources & evidence

ORD record
ord-af5d07b5001c43b5a524887b19ad5962
Source dataset
uspto-grants-1991_01
Patent number
US04985417

Reaction notes

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