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

Hydrochloric Acid → 5-[7-(3-Diethylamino-propionyl)-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidin-4-yloxy]-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide

HRID 205821
Notes
Print preview

Reaction equation

HRID 205821 reaction equation
[CH2:68]([CH3:69])[N:70]([CH2:71][CH2:72][C:73](=[O:74])[OH:75])[CH2:76][CH3:77].[CH:58]([N:59]([CH2:60][CH3:61])[CH:62]([CH3:63])[CH3:64])([CH3:65])[CH3:66].[ClH:67].[F:1][C:2]([c:3]1[cH:4][c:5]([NH:9][C:10](=[O:11])[n:12]2[cH:13][cH:14][c:15]3[cH:16][c:17]([O:21][c:22]4[c:23]5[c:24]([n:25][cH:26][n:27]4)[CH2:28][NH:29][CH2:30][CH2:31]5)[cH:18][cH:19][c:20]23)[cH:6][cH:7][cH:8]1)([F:32])[F:33].[O:78]=[CH:79][N:80]([CH3:81])[CH3:82].[P-:34]([F:35])([F:36])([F:37])([F:38])([F:39])[F:40].[n:41]1([O:42][C:43]([N:44]([CH3:45])[CH3:46])=[N+:47]([CH3:48])[CH3:49])[c:50]2[n:51][cH:52][cH:53][cH:54][c:55]2[n:56][n:57]1>>[F:1][C:2]([c:3]1[cH:4][c:5]([NH:9][C:10](=[O:11])[n:12]2[cH:13][cH:14][c:15]3[cH:16][c:17]([O:21][c:22]4[c:23]5[c:24]([n:25][cH:26][n:27]4)[CH2:28][N:29]([C:73]([CH2:72][CH2:71][N:70]([CH2:68][CH3:69])[CH2:76][CH3:77])=[O:74])[CH2:30][CH2:31]5)[cH:18][cH:19][c:20]23)[cH:6][cH:7][cH:8]1)([F:32])[F:33]
ParticipantsSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 9886HexafluorophosphateHCID 81531DiisopropylethylamineHCID 247454N,N-Diethyl-beta-alanineHCID 4641409(Dimethylamino)-N,N-dimethyl(3H-(1,2,3)triazolo(4,5-b)pyridin-3-yloxy)methaniminium
HCID 46224262
5-(5,6,7,8-Tetrahydro-pyrido[3,4-d]pyrimidin-4-yloxy)-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide

Product 1

HCID 593945005-[7-(3-Diethylamino-propionyl)-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidin-4-yloxy]-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide

Sources & evidence

ORD record
ord-4860e0c0b7924e2e8d50df2ded9b5fd1
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

Loading…

On this pageParticipantsSources & evidenceReaction notes