HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624543Generated: October 31, 2026
HCID 136377197, compound → HCID 136252346, compound
https://huagongshe.com/reaction/624543
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 136377197 | HCID 136377197 | — |
| Solvent | Methylamine | HCID 6329 | — |
| Product | HCID 136252346 | HCID 136252346 | — |
Reaction Steps
A solution of 2-((1-methyl-4-(2-methyl-10H-benzo[b]thieno[2,3-e][1,4]diazepin-4-yl)piperazin-2-yl)methyl)isoindoline-1,3-dione, prepared as described in the previous step, (1.0 g) in ethanolic methylamine (20 mL) was stirred at ambient temperature overnight. The solvent was removed under vacuum and the residue purified by HPLC to give the hydrochloride salt of (1-methyl-4-(2-methyl-10H-benzo[b]thieno[2,3-e][1,4]diazepin-4-yl)piperazin-2-yl)methanamine as a red solid. 1H NMR (400 MHz, MeOD) δ 7.46-7.44 (m, 1H), 7.31-7.48 (m, 1H), 7.19-7.15 (m, 1H), 6.97-6.95 (m, 1H), 6.74 (s, 1H), 4.80-4.71 (br, 1H), 4.28-4.20 (br, 2H), 4.07-4.04 (br, 2H), 3.82-3.70 (br, 3H), 3.53-3.48 (m, 1H), 3.18 (s, 3H), 2.42 (m, 3H); ESI-MS (M+1): 342 calc. for C18H23N5S Exact Mass: 341.17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303041B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-c8bff0b135704d88a4ef08256ffda253 |
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| Source note | uspto-grants-2016_04 |
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