Isopropylamine → (RS)-4-Chloro-N-isopropyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidine-7-carboxamide
Reaction equation
[Cl:1][C:2]1[C:3]2[C:10]3[CH2:11][CH2:12][CH:13]([C:15]([OH:17])=O)[CH2:14][C:9]=3[S:8][C:4]=2[N:5]=[CH:6][N:7]=1.[CH3:18][CH:19]([NH2:21])[CH3:20]>>[Cl:1][C:2]1[C:3]2[C:10]3[CH2:11][CH2:12][CH:13]([C:15]([NH:21][CH:19]([CH3:20])[CH3:18])=[O:17])[CH2:14][C:9]=3[S:8][C:4]=2[N:5]=[CH:6][N:7]=1Participants
3
Procedure
13.18 g (49.05 mmol) (RS)-4-chloro-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidine-7-carboxylic acid (prepared according to intermediate example 31b) were transformed in analogy to example 3 using propan-2-amine to give after working up and purification 11.39 g (71%) of the title compound.
Workup
- customto give
- custompurification 11.39 g (71%) of the title compound
Sources & evidence
- ORD record
- ord-7290af837b1245b1a6ccdca97d62cbad
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296757B2
Reaction notes
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