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

Thenyl mercaptan → 4-[[-2-Hydroxy-1-(hydroxymethyl)ethyl]amino]-2-[(2-thienylmethyl)thio]-7(8h)-pteridinone

HRID 1814262
Notes
Print preview

Reaction equation

HRID 1814262 reaction equation
F[C:2]1[C:7](F)=[CH:6]C=C[C:3]=1[CH2:9][S:10]([C:13]1[N:22]=[C:21]([NH:23][CH:24]([CH2:27][OH:28])[CH2:25][OH:26])[C:20]2[N:19]=[CH:18][C:17](=[O:29])[NH:16][C:15]=2[N:14]=1)(=O)=O.[S:30]1C=CC=C1CS>>[OH:26][CH2:25][CH:24]([NH:23][C:21]1[C:20]2[N:19]=[CH:18][C:17](=[O:29])[NH:16][C:15]=2[N:14]=[C:13]([S:10][CH2:9][C:3]2[S:30][CH:6]=[CH:7][CH:2]=2)[N:22]=1)[CH2:27][OH:28]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 80408Thenyl mercaptanHCID 225059372-[[(2,3-Difluorophenyl)methyl]sulfonyl]-4-[[-2-hydroxy-1-hydroxymethylethyl]amino]-7(8H)-pteridinone

Product 1

HCID 225059754-[[-2-Hydroxy-1-(hydroxymethyl)ethyl]amino]-2-[(2-thienylmethyl)thio]-7(8h)-pteridinoneYield 53.5%

Procedure

The titled compound (0.075 g) was prepared by the method of Example 13, step (c) using the product from example 23, step (a) (0.21 g) and 2-thienylmethylmercaptan (0.05 g).

Sources & evidence

ORD record
ord-3d6d53405d4e45938237d05d0c8b5a93
Source dataset
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06875868B2

Reaction notes

Loading…

On this pageParticipantsProcedureSources & evidenceReaction notes