Hydrochloric Acid → HCID 11394505, compound

HRID 2414677Notes

Reaction equation

HRID 2414677 reaction equation
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([S:12]([N:15]2[CH:21]([C:22]([NH:24][OH:25])=[O:23])[CH2:20][CH2:19][N:18](C(OC(C)(C)C)=O)[CH2:17][CH2:16]2)(=[O:14])=[O:13])=[CH:8][CH:7]=1)[C:2]#[C:3][CH3:4].Cl>O1CCOCC1>[CH2:1]([O:5][C:6]1[CH:7]=[CH:8][C:9]([S:12]([N:15]2[CH:21]([C:22]([NH:24][OH:25])=[O:23])[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]2)(=[O:13])=[O:14])=[CH:10][CH:11]=1)[C:2]#[C:3][CH3:4]

Participants

4

Procedure

To the product of Example 291, tert-butyl 4-{[4-(2-butynyloxy)phenyl]-sulfonyl}-5-[(hydroxyamino)carbonyl]-1,4-diazepane-1-carboxylate (0.32 g, 0.68 mmol), was added 4N hydrochloric acid in dioxane (9 mL) After 10 min the reaction mixture was concentrated in vacuo. Trituration of the residue with diethyl ether gave 4-{[4-(2-butynyloxy)phenyl]sulfonyl}-N-hydroxy-1,4-diazepane-5-carboxamide as an off-white powder (0.27 g). Electrospray Mass Spec 368.2 (M+H)+

Workup

  1. concentrationwas concentrated in vacuo

Sources & evidence

ORD record
ord-bc942b880eef4eac99d4456c98a16bc9
Source dataset
uspto-grants-2004_11
Patent number
US06812227B2

Reaction notes

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