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

4-Methoxybutanoyl chloride → tert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(4-methoxybutyrylamino)benzyloxy]piperidine-1-carboxylate

HRID 2326387
Notes
Print preview

Reaction equation

HRID 2326387 reaction equation
[CH3:43][O:44][CH2:45][CH2:46][CH2:47][C:48](=[O:49])[Cl:50].[NH2:1][c:2]1[c:3]([CH2:4][O:5][CH:6]2[CH2:7][N:8]([C:32](=[O:33])[O:34][C:35]([CH3:36])([CH3:37])[CH3:38])[CH2:9][CH2:10][CH:11]2[c:12]2[cH:13][cH:14][c:15]([O:18][CH2:19][CH2:20][CH2:21][O:22][CH2:23][c:24]3[c:25]([O:30][CH3:31])[cH:26][cH:27][cH:28][cH:29]3)[cH:16][cH:17]2)[cH:39][cH:40][cH:41][cH:42]1>>[NH:1]([c:2]1[c:3]([CH2:4][O:5][CH:6]2[CH2:7][N:8]([C:32](=[O:33])[O:34][C:35]([CH3:36])([CH3:37])[CH3:38])[CH2:9][CH2:10][CH:11]2[c:12]2[cH:13][cH:14][c:15]([O:18][CH2:19][CH2:20][CH2:21][O:22][CH2:23][c:24]3[c:25]([O:30][CH3:31])[cH:26][cH:27][cH:28][cH:29]3)[cH:16][cH:17]2)[cH:39][cH:40][cH:41][cH:42]1)[C:48]([CH2:47][CH2:46][CH2:45][O:44][CH3:43])=[O:49]
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 127949894-Methoxybutanoyl chlorideHCID 68506158Tert-butyl 3-(2-aminobenzyloxy)-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate

Product 1

HCID 68502090tert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(4-methoxybutyrylamino)benzyloxy]piperidine-1-carboxylate

Sources & evidence

ORD record
ord-9d226ed3843244b1aa2a3c0b949aec8f
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI
10.1039/C8SC04228D

Reaction notes

Loading…

On this pageParticipantsSources & evidenceReaction notes