Hydrochloric Acid → HCID 58413161, compound

HRID 240657Notes

Reaction equation

HRID 240657 reaction equation
C[O:2][C:3]([C:5]1[S:27][C:8]2[N:9]=[CH:10][N:11]=[C:12]([NH:13][C:14]3[C:15]([O:20][C@@H:21]4[CH2:26][CH2:25][CH2:24][O:23][CH2:22]4)=[N:16][CH:17]=[CH:18][CH:19]=3)[C:7]=2[C:6]=1[CH3:28])=[O:4].CO.[OH-].[Na+].Cl>O.C1COCC1>[CH3:28][C:6]1[C:7]2[C:12]([NH:13][C:14]3[C:15]([O:20][C@@H:21]4[CH2:26][CH2:25][CH2:24][O:23][CH2:22]4)=[N:16][CH:17]=[CH:18][CH:19]=3)=[N:11][CH:10]=[N:9][C:8]=2[S:27][C:5]=1[C:3]([OH:4])=[O:2]

Participants

7

Procedure

A mixture of 1.4 g (3.14 mmol) 5-methyl-4-{2-[(R)-(tetrahydro-pyran-3-yl)oxy]-pyridin-3-ylamino}-thieno[2,3-d]pyrimidine-6-carboxylic acid methyl ester, 20 ml methanol, 7 ml THF and 6.29 ml sodium hydroxid solution (1 M) was stirred at room temperature for 48 hours. Then 6.3 ml hydrochloric acid solution (1M) were added followed by addition of water. The mixture was filtered. The solid was washed with water and diisopropylether and dried in an oven (vacuo).

Workup

  1. filtrationThe mixture was filtered
  2. washThe solid was washed with water and diisopropylether
  3. customdried in an oven (vacuo)

Sources & evidence

ORD record
ord-a3840c4d87a74ed19b0b948ca86a5636
Source dataset
uspto-grants-2014_02
Patent number
US08648068B2

Reaction notes

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