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

4-Benzyloxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl ester → 4-Hydroxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl ester

HRID 250494
Notes
Print preview

Reaction equation

HRID 250494 reaction equation
[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=2)[C:11]2[C:16]([C:17]=1[O:18]CC1C=CC=CC=1)=[CH:15][CH:14]=[CH:13][CH:12]=2)=[O:7])[CH2:2][CH2:3][CH3:4].C1C=CC(C([C@@H]2OC[C@H](NCC3C=CC(F)=CC=3)C(O)C2)C2C=CC=CC=2)=CC=1>>[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=2)[C:11]2[C:16]([C:17]=1[OH:18])=[CH:15][CH:14]=[CH:13][CH:12]=2)=[O:7])[CH2:2][CH2:3][CH3:4]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 667133694-Benzyloxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl esterHCID 71452722D-153 (FDA NDC: 58264-0164)

Product 1

HCID 1363603074-Hydroxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl ester

Procedure

Synthesized from 4-Benzyloxy-1-pyridin-2-yl-isoquinoline-3-carboxylic acid butyl ester in analogy to example D-153 b); MS-(−)-ion M−1=321.4.

Sources & evidence

ORD record
ord-8627020df7524d03a22dcc95f7ccdcb4
Source dataset
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07863292B2

Reaction notes

Loading…

On this pageParticipantsProcedureSources & evidenceReaction notes