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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1687778Generated: November 2, 2026

8-Amino-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one → HCID 66830439, compound

https://huagongshe.com/reaction/1687778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Amino-1,3,4,5-tetrahydro-2H-1-benzazepin-2-oneHCID 4615168—
ReactantHCID 86634034HCID 86634034—
ProductHCID 66830439HCID 66830439—

Reaction Steps

2-[5-Chloro-2-(2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-8-ylamino)-pyrimidin-4-ylamino]-5-dimethylamino-N-methyl-benzamide was prepared from 8-amino-1,3,4,5-tetrahydro-benzo[b]azepin-2-one and 2-(2,5-dichloro-pyrimidin-4-ylamino)-5-dimethylamino-N-methyl-benzamide in an analogous manner to Example 1410. Product isolated as a yellow solid (155 mg, 81%). m.p.=253-255° C.; LCMS (m/e) 480 (M+H); 1HNMR (d6-DMSO, 400 MHz) δ 11.46 (bs, 1H), 9.80-9.66 (m, 1H), 9.51 (s, 1H), 8.87-8.77 (m, 1H), 8.53-8.40 (m, 1H), 8.21 (s, 1H), 7.34 (s, 1H), 7.29-7.09 (m, 1H), 7.25 (d, 1H, J=8.0 Hz), 7.17 (d, 1H, J=8.5 Hz), 7.03-6.81 (m, 1H), 2.99 (s, 6H), 2.81 (d, 3H, J=3.8 Hz), 2.65 (t, 2H, J=6.8 Hz), 2.24-2.15 (m, 2H), 2.15-2.04 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148391B2
Source datasetuspto-grants-2012_04
ORD IDord-27c1d8b218cf4eba9d30e8155aa06925
Source noteuspto-grants-2012_04