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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1687142Generated: October 30, 2026

2-(2,5-Dichloropyrimidin-4-ylamino)-N-methylbenzamide → HCID 66830229, compound

https://huagongshe.com/reaction/1687142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2,5-Dichloropyrimidin-4-ylamino)-N-methylbenzamideHCID 57974132—
ReactantHCID 67264544HCID 67264544—
ProductHCID 66830229HCID 66830229—

Reaction Steps

2-{5-Chloro-2-[3-((S)-3,3,3-trifluoro-2-methoxy-propyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]-pyrimidin-4-ylamino}-N-methyl-benzamide was prepared from 3-((S)-3,3,3-trifluoro-2-methoxy-propyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamine and 2-(2,5-dichloro-pyrimidin-4-ylamino)-N-methyl-benzamide in an analogous manner to Example 328c. Product isolated as a yellow solid (57 mg, 26%). m.p.=160-162° C.; LCMS (m/e) 549 (M+1); 1H-NMR (CDCl3, 400 MHz) δ 11.08 (s, 1H), 8.68 (d, 1H, J=8.5 Hz), 8.11 (s, 1H), 7.50 (d, 1H, J=7.9 Hz), 7.48-7.42 (m, 1H), 7.36 (s, 1H), 7.30-7.25 (m, 1H), 7.13-7.07 (m, 1H), 7.04 (d, 1H, J=8.0 Hz), 3.76-3.67 (m, 1H), 3.62 (s, 3H), 3.06 (d, 3H, J=4.7 Hz), 2.94-2.86 (m, 4H), 2.86-2.82 (m, 2H), 2.79-2.73 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148391B2
Source datasetuspto-grants-2012_04
ORD IDord-e6f37321a742492bbcb9426f4d4f62bf
Source noteuspto-grants-2012_04