HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

N,1-dimethylindole-2-carboxamide → 5-Benzyloxy-1-methyl-2-(methylaminomethyl)indole

HRID 1633841
Notes
Print preview

Reaction equation

HRID 1633841 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14]([CH3:18])[C:13]([C:19]([NH:21][CH3:22])=O)=[CH:12]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CNC(C1N(C)C2C(C=1)=CC=CC=2)=O>>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14]([CH3:18])[C:13]([CH2:19][NH:21][CH3:22])=[CH:12]2)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 12303315N,1-dimethylindole-2-carboxamideHCID 149059755-benzyloxy-N,1-dimethylindole-2-carboxamide

Product 1

HCID 149059815-Benzyloxy-1-methyl-2-(methylaminomethyl)indoleYield 69%

Procedure

According to the procedure of Preparation 1(b), except substituting 5-benzyloxy-N,1-dimethylindole-2-carboxamide (37.4 g, 126.7 mmole) for the N,1-dimethylindole-2-carboxamide, the title compound (24.5 g, 69%) was prepared as a white solid: MS (ES) m/e 281 (M+H)+.

Sources & evidence

ORD record
ord-e4b91edc241b478a9199de9aa045f91f
Source dataset
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06503903B1

Reaction notes

Loading…

On this pageParticipantsProcedureSources & evidenceReaction notes