HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686949Generated: October 30, 2026
HCID 58236399, compound → HCID 66830220, compound
https://huagongshe.com/reaction/1686949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58236399 | HCID 58236399 | — |
| Reactant | 1022959-73-4 | HCID 67265274 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 66830220 | HCID 66830220 | — |
Reaction Steps
Following the procedure of Example 101b, 1-Methyl-2,3,4,5-tetrahydro-1H-benzo[b]azepin-7-ylamine (48 mgs, 0.27 mmol) and N-[2-(2,5-Dichloro-pyrimidin-4-ylamino)-phenyl]-methanesulfonamide (0.9 eq) were reacted except that the ISCO chromatography gradient was 0% to 10% MeOH/CH2Cl2 and the final product was triturated from 4 mL of EtOAc with hexane to give N-{2-[5-Chloro-2-(1-methyl-2,3,4,5-tetrahydro-1H-benzo[b]azepin-7-ylamino)-pyrimidin-4-ylamino]-phenyl}-methanesulfonamide (30.6 mgs) as an off-white/grey solid. MP=170-172° C. 1H-NMR (CDCl3) δ δ 7.88 (s, 1H), 7.50-7.48 (m, 1H), 7.36-7.33 (m, 1H), 7.23 (s, 1H), 7.17-7.13 (m, 2H), 6.95-6.89 (m, 3H), 6.68 (s, 1H), 6.63 (br s, 1H), 2.71-2.68 (m, 8H), 2.50-2.47 (m, 2H), 1.63-1.55 (m, 2H), 1.42-1.38 (m, 2H); LC/MS (ESI+): 273 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148391B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-4700ac0802a8423fa5cbad4dfb439cdf |
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| Source note | uspto-grants-2012_04 |
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