Hydrochloric Acid → HCID 22674466, compound
Reaction equation
C(OC([NH:8][CH2:9][CH2:10][NH:11][C:12]1[N:13]=[C:14]([C:21]([C:23]2[S:24][CH:25]=[CH:26][CH:27]=2)=[O:22])[C:15]2[S:20][CH:19]=[CH:18][C:16]=2[N:17]=1)=O)CCC.[ClH:28]>CO.O1CCOCC1>[ClH:28].[ClH:28].[NH2:8][CH2:9][CH2:10][NH:11][C:12]1[N:13]=[C:14]([C:21]([C:23]2[S:24][CH:25]=[CH:26][CH:27]=2)=[O:22])[C:15]2[S:20][CH:19]=[CH:18][C:16]=2[N:17]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 2-(2-butoxycarbonylaminoethylamino)thieno[3,2-d]pyrimidin-4-yl 2-thienylmethanone (58 mg, 0.14 mmol) in MeOH (5 mL) was treated with 4-M HCl in dioxane (0.5 mL), stirred at room temperature for 16 h and the resulting solid filtered and washed with ether to give the title compound (41 mg, 77%) as a white crystalline solid.
Workup
- filtrationthe resulting solid filtered
- washwashed with ether
Sources & evidence
- ORD record
- ord-6e75937168a246419193d4998cb1c85a
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06787541B1
Reaction notes
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