Methylamine hydrochloride → HCID 58659650, compound

HRID 1676979Notes

Reaction equation

HRID 1676979 reaction equation
ClC1C=C2[C:8](=CC=1)[N:7](S(C1C=CC=CC=1)(=O)=O)C(C(OCC)=O)=C2S(Cl)(=O)=O.[Br:29][C:30]1[CH:31]=[C:32]2[C:36](=[CH:37][CH:38]=1)[N:35](S(C1C=CC=CC=1)(=O)=O)[C:34]([C:48](OCC)=[O:49])=[C:33]2[S:53](Cl)(=[O:55])=[O:54].Cl.CN.Cl.C[NH:62]CCC(OC)=O>>[Br:29][C:30]1[CH:31]=[C:32]2[C:36](=[CH:37][CH:38]=1)[NH:35][C:34]([C:48]([NH2:62])=[O:49])=[C:33]2[S:53]([NH:7][CH3:8])(=[O:55])=[O:54]

Participants

5

Reactant 4

HCID 6364545Methylamine hydrochlorideHCID 12414199methyl 3-(methylamino)propanoate hydrochlorideHCID 22401482ethyl 5-chloro-3-(chlorosulfonyl)-1-(phenylsulfonyl)-1H-indole-2-carboxylateHCID 86592455ethyl 3-(chlorosulfonyl)-5-bromo-1-(phenylsulfonyl)-1H-indole-2-carboxylate

Product 1

HCID 58659650HCID 58659650, compound

Procedure

Following the procedures described in Steps D and E of Example 1, replacing in Step D ethyl 5-chloro-3-(chlorosulfonyl)-1-(phenylsulfonyl)-1H-indole-2-carboxylate with ethyl 5-bromo-3-(chlorosulfonyl)-1-(phenylsulfonyl)-1H-indole-2-carboxylate, and methylamine hydrochloride with methyl N-methyl-β-alaninate hydrochloride, the title compound was obtained. Proton NMR for the product was consistent with the titled compound. ESI+ MS: 332.2 [M+H]+.

Sources & evidence

ORD record
ord-141bdceea233427dab36a5bd8113a60a
Source dataset
uspto-grants-2011_08
Patent number
US08008295B2

Reaction notes

Loading…