Hydrochloric Acid → HCID 23048744, compound
Reaction equation
Cl[C:2]([N:4]1[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[NH:8][C:7](=[O:15])[C:6]2=[CH:16][S:17][C:18]([CH3:19])=[C:5]12)=[O:3].[N:20]1([CH2:26][CH2:27][CH:28]2[O:33][CH2:32][CH2:31][NH:30][CH2:29]2)[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1.Cl>>[CH3:19][C:18]1[S:17][CH:16]=[C:6]2[C:7](=[O:15])[NH:8][C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[N:4]([C:2]([N:30]3[CH2:31][CH2:32][O:33][CH:28]([CH2:27][CH2:26][N:20]4[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]4)[CH2:29]3)=[O:3])[C:5]=12Participants
4
Procedure
Prepared analogously to Example 4 from 4-(chlorocarbonyl)-4,9-dihydro-3-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one and 2-[2-(1-piperidinyl)ethyl]morpholine in a yield of 74% of theory. Rf 0.48 (conditions as in Example 58). The colourless hydrochloride melted at 254°-256° C. (D.).
Sources & evidence
- ORD record
- ord-faa9d0f4e3524616b89e4f06f9d1a53f
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04931436
Reaction notes
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