Hydroxyamine hydrochloride → HCID 11012667, compound

HRID 2305869Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([C:12]([CH2:19][C:20]#[CH:21])([CH2:16][C:17]#[CH:18])[C:13](O)=[O:14])(=[O:11])=[O:10])=[CH:5][CH:4]=1.Cl.[NH2:23][OH:24]>>[OH:24][NH:23][C:13](=[O:14])[C:12]([S:9]([C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)(=[O:11])=[O:10])([CH2:19][C:20]#[CH:21])[CH2:16][C:17]#[CH:18]

Participants

Reactant 2

HCID 443297Hydroxyamine hydrochloride

HCID 11023162HCID 11023162, compound

Product 1

HCID 11012667HCID 11012667, compoundYield 85%

Procedure

2-(4-Methoxy-benzenesulfonyl)-2-prop-2-ynyl-pent4ynoic acid hydroxyamide was prepared according to the method as outlined in Example 1. Starting from (4methoxy-benzenesulfonyl)-2-prop-2-ynyl-pent-4-ynoic acid (0.25 g, 0.81 minol) and hydroxylamine hydrochloride (0.70 g, 10 mmol), 0.22 g of the product was isolated. Yield 85%; white solid; mp 156° C.; MS: 321.9 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 2.00-2.13 (m, 2H), 3.00-3.30 (m, 4H), 3.90(s, 3H), 7.01 (d, J=9.0 Hz, 2H), 7.82 (d, J =9.0 Hz, 2H), 8.76 (brs, 1H), 10.65 (brs, 1H); IR (KBr, cm-1): 3392s, 3293s, 3271m, 2955m, 1650s, 1594s; Anal. Calc'd for C15H15NO5S: C, 56.07; H, 4.70; N, 4.36.

Sources & evidence

ORD record: ord-14aaa0cf2bdf458f85b7f78edc350c04
Source dataset: uspto-grants-2002_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06441023B1

Reaction notes

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