7-Chloro-5-[[(2,3-difluorophenyl)methyl]thio]-thiazolo[4,5-d]pyrimidin-2-amine → (+/-)-2-[[2-Amino-5-[[(2,3-difluorophenyl)methyl]thio]thiazolo[4,5-d]pyrimidin-7-yl]amino]-3-methoxy-1-propanol

HRID 1097369Notes

Reaction equation

HRID 1097369 reaction equation
Cl[C:2]1[C:3]2[S:20][C:19]([NH2:21])=[N:18][C:4]=2[N:5]=[C:6]([S:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[C:11]=2[F:17])[N:7]=1.Cl.[NH2:23][CH:24]([CH2:27][O:28][CH3:29])[CH2:25][OH:26]>>[NH2:21][C:19]1[S:20][C:3]2[C:2]([NH:23][CH:24]([CH2:27][O:28][CH3:29])[CH2:25][OH:26])=[N:7][C:6]([S:8][CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[C:11]=3[F:17])=[N:5][C:4]=2[N:18]=1

Participants

3

Reactant 2

HCID 112216507-Chloro-5-[[(2,3-difluorophenyl)methyl]thio]-thiazolo[4,5-d]pyrimidin-2-amineHCID 729960102-Amino-3-methoxypropan-1-ol hydrochloride

Product 1

HCID 86635806(+/-)-2-[[2-Amino-5-[[(2,3-difluorophenyl)methyl]thio]thiazolo[4,5-d]pyrimidin-7-yl]amino]-3-methoxy-1-propanol

Procedure

Prepared by the method of example 12 step a) using the product of example 4 step b) and the product of example 40 step a).

Workup

  1. customPrepared by the method of example 12 step a)

Sources & evidence

ORD record
ord-a7a272452bd24a1a939f081cabbcc7f9
Source dataset
uspto-grants-2012_03
Patent number
US08143261B2

Reaction notes

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