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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041005Generated: October 31, 2026

7-morpholino-6,7,8,9-tetrahydro-5H-benzo[7]annulen-3-amine → HCID 66830680, compound

https://huagongshe.com/reaction/1041005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-morpholino-6,7,8,9-tetrahydro-5H-benzo[7]annulen-3-amineHCID 57416136—
ReactantHCID 57522618HCID 57522618—
ProductHCID 66830680HCID 66830680—

Reaction Steps

In an analogous procedure to Example 651, part c, 7-Morpholin-4-yl-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-ylamine and (1S,2S,3R,4R)-3-(2,5-Dichloro-pyrimidin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide were combined to yield 1S,2S,3R,4R)-3-[5-Chloro-2-(7-morpholin-4-yl-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-ylamino)-pyrimidin-4-ylamino]-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide as a white solid. 1H-NMR (CDCl3) δ 9.12 (s, 1H), 7.93 (s, 1H), 7.78 (s, 1H), 7.70 (m, 1H), 7.52 (m, 1H), 7.46 (d, J=21.2 Hz, 1H), 7.26 (s, 1H), 7.00 (d, J=8.2 Hz, 1H), 6.35 (s, 1H), 6.27 (s, 1H), 4.13 (m, 1H), 3.31 (s, 3H), 2.87 (s, 1H), 2.77 (s, 1H), 2.56 (m, 6H), 2.45 (m, 4H), 2.10 (d, J=8.6 Hz, 1H), 1.95 (m, 2H), 1.40 (d, J=8.8 Hz, 1H), 1.31 (m, 2H). LC/MS (ESI+)=509 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-693111492a704ac3b55b5501e5920181
Source noteuspto-grants-2013_10