Oxalate → HCID 9844212, compound

HRID 1376569Notes

Reaction equation

[CH2:1]([NH:4][CH2:5][CH:6]1[CH2:15][CH2:14][C:13]2[C:8](=[CH:9][C:10]([NH:16][S:17]([CH3:20])(=[O:19])=[O:18])=[CH:11][CH:12]=2)[O:7]1)[CH2:2][CH3:3].[C:21]([O-:26])(=O)[C:22]([O-])=O>>[NH2:16][C:10]1[CH:11]=[C:21]([CH:22]=[CH:8][CH:9]=1)[O:26][CH2:3][CH2:2][CH2:1][NH:4][CH2:5][CH:6]1[CH2:15][CH2:14][C:13]2[C:8](=[CH:9][C:10]([NH:16][S:17]([CH3:20])(=[O:18])=[O:19])=[CH:11][CH:12]=2)[O:7]1

Participants

Reactant 2

HCID 71081Oxalate

HCID 22917826HCID 22917826, compound

Product 1

HCID 9844212HCID 9844212, compound

Procedure

N-(2-Propylaminomethyl-chroman-7-yl)-methanesulfonamide as the oxalate, hemihydrate, mp 204°-205° C.

Sources & evidence

ORD record: ord-c5904ea5202041b29808da96197cbcd5
Source dataset: uspto-grants-1997_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05663194

Reaction notes

Loading…